General Electric Company — Medical Systems Group (GE) appeals the judgment of the United States Court of International Trade,
General Elec. Co.
—Med.
Sys. Group v. United States,
Background
Between 1992 and 1994, GE imported 98 multiformat cameras (MFCs), 97 of which were for use solely with computerized tomography (CT) x-ray scanners. One MFC, of a different model, was for use with a magnetic resonance imaging (MRI) system. A MFC is an apparatus containing an internal cathode-ray-tube monitor that displays a computer-generated image and a camera assembly that photographs *1233 the monitor’s display screen. When connected to the CT or MRI system, the computer-generated image created from the CT system’s x-rays or the MRI system’s magnetic resonances is transmitted to the MFC’s display monitor. The camera lens is aimed at the screen monitor in order to photograph the screen and the displayed image. The MFC produces a hard-copy photograph on x-ray film. The term “multiformat” refers to the apparatus’ ability to produce multiple images on a single sheet of x-ray film. Because of the electro-magnetic field produced by the MRI system, MFC models designed for use in CT systems cannot be used with MRI systems. The cathode-ray-tube monitor assembly in the MFC model for MRI systems is enclosed in a metal protective shield.
Although the manufacturer sets the lens assembly of the MFC in a fixed position, there are several ways to adjust its output quality. The internal display monitor has an adjustment knob accessible to the system operator. This affects the finished photograph because the camera records the image displayed on the screen. In addition, the distance between the lens and the film plane in the camera assembly, and thereby the picture quality, may be adjusted by inserting or removing washers. Finally, the focus ring on the unit’s “small image” lens may be adjusted by removing a factory installed silicone seal. These last two adjustments are intended to be performed only by a trained service engineer during periodic maintenance scheduled every three months.
The primary issue in this case is the proper classification under the Harmonized Tariff Schedule of the United States (HTSUS) for the 97 MFCs used exclusively in CT systems. The parties dispute which of the following headings and subheadings constitute the proper classification for MFCs:
9006 Photographic (other than cinematographic) cameras; ...:
Other cameras:
9006.59 Other:
9006.59.40 Fixed focus ... Other than fixed focus:
9006.59.90 Valued over $10 each 9022 Apparatus based on the use of X-rays ..., including ... X-ray tubes and other X-ray generators, ... control panels and desks, screens, examination or treatment tables, chairs and the like; parts and accessories thereof:
9022.90 Other, including parts and accessories:
Parts and accessories:
Other: 9022.90.60 Of apparatus based on the use of X-rays
HTSUS (1992 ed. Supp. 1).
Customs classified the MFCs under subheading 9006.59.40 as fixed focus cameras. GE timely protested the classification, which Customs denied, and GE challenged the classification in the Court of International Trade. GE claimed that the MFCs are more properly classified under subheading 9006.59.90, as other than fixed *1234 focus cameras valued at over $10 each. In the alternative, 6E claimed that the MFCs should be classified under subheading 8479.89.90, as other machines and mechanical appliances having individual functions, not specified or included elsewhere in this chapter.
GE moved for partial summary judgment on the 9006.59.90 claim and Customs cross-moved for summary judgment dismissing both of GE’s claims. In its reply, GE did not oppose Customs’ cross-motion as to the 8479.89.90 claim, but filed a proposed amended consolidated complaint that incorporated a new claim. It based the new claim in-part on statements in Customs’ reply brief that the display monitor is separate from the camera assembly. GE argued that because the MFCs contain both a camera and a display monitor separate from the camera, they are a combination apparatus, and are properly classified under subheading 9022.90.60 as parts and accessories, other, of apparatus based on the use of x-rays.
GE did not file a formal motion to amend its complaint under local rule 15(a) and did not amend its motion for partial summary judgment. Its reply brief argued that the 9022.90.60 claim had been litigated with the implied or express consent of the defendant, and, therefore, under local rule 15(b), the pleading should be amended to conform to the evidence. In its reply brief, Customs addressed GE’s 9022.90.60 claim and both parties discussed the claim in their post-argument briefs.
The Court of International Trade declined to consider the amended complaint under local rule 15(a). In addition, the court rejected GE’s argument that it should amend the pleadings to conform to the evidence under local rule 15(b). The court stated that rule 15(b) only applies when a trial has been or is being held, not when summary judgment was entered before trial. However, the court recognized its duty, under
Jarvis Clark Co. v. United States,
Discussion
We review the court’s grant of summary judgment without deference.
See Mead Corp. v. United States,
The proper classification of merchandise is governed by the General Rules of Interpretation (GRI) to the HTSUS.
See Orlando Food Corp. v. United States,
The trial court first determined that the MFCs for CT systems did not fall within the terms of heading 9022 for parts and accessories which are “solely or principally” for use with x-ray apparatus.
Although an accessory to an apparatus classified under heading 9022, Note 2(a) to HTSUS Chapter 90 further provides that “[p]arts and accessories which are goods included in any of the headings of this chapter ... are in all cases to be classified in their respective headings.” Explanatory Note 1(A)(3) to heading 9022 provides that separately presented cameras, even if specially designed for use with an x-ray apparatus, are classified in heading 9006 because the camera is a “good” included in a separate heading of Chapter 90. Therefore, to be classifiable under heading 9022 as accessories, MFCs must not be classifiable as “cameras” in heading 9006.
The MFCs presented by GE are combination apparatuses. The camera is only part of a combination, which includes a camera assembly and a functionally separate internal display monitor. Both - the display monitor and the camera must independently perform their nonsubordinate functions if the MFC is to operate properly. Although Chapter Note 2(a) requires separately imported cameras, even if accessories of x-ray apparatuses, to be classified under heading 9006, it does not include combination apparatuses in which merely one component is a camera. GRI 3(a) states that the heading that provides the most specific description shall be preferred. A heading that describes the entire apparatus as a single unit is more specific than a heading describing one component of a combination apparatus. Because a MFC is a combination apparatus that is an accessory to an apparatus based on the use of x-rays, heading 9022 provides the most specific description.
*1236
Customs argues that the MFCs cannot be classified under 9022 because the device, as imported, does not generate any x-rays. The Explanatory Notes, Customs argues, indicate that the only cameras included in the heading are those imported with an x-ray apparatus. Because neither the monitor nor camera produce x-rays, and MFCs are not presented with an apparatus that produces x-rays, the merchandise cannot be classified under heading 9022. This argument, however, places too much weight on the non-binding Explanatory Notes.
See Mita Copystar Am. v. United States,
The MFC for MRI systems is identical to the MFC for CT systems except for the protective shield. However, GE concedes that that MFC cannot be classified in heading 9022, since an MRI scanner is not based on the use of x-rays. Customs argues that because the MFC designed for MRI systems is not solely or principally used with an apparatus under heading 9022, the MFC is properly classified in the residual heading 9033 by application of Note 2(c) to Chapter 90. The MFC model in question, however, was designed principally for use with MRI systems. Under Note 2(b) to Chapter 90, parts or accessories suitable for use solely or principally with a particular apparatus are to be classified under the same heading. Heading 9018 provides a classification for “[[Instruments and appliances used in medical ... sciences, including ... other electro-medical apparatus and ... parts and accessories thereof.” Therefore, the remaining MFC dedicated for use in MRI systems is properly classified under subheading 9018.90.80, as “[o]ther instruments and appliances and parts and accessories thereof: other: other.” *
Conclusion
Accordingly, we reverse the judgment of the Court of International Trade.
Notes
In light of our disposition, we need not reach GE's argument that the Court of International Trade committed prejudicial error by failing to amend the pleadings to conform to the evidence under local rule 15(b).
