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FDA 510(k)

3-CCD DIGITAL CAMERA SYSTEM

K-Number: K031098 · 2003-06-04

ApplicantLinvatec Corp.
Decision Date2003-06-04
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

3-CCD DIGITAL CAMERA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Linvatec Corp.. It received FDA 510(k) clearance on 2003-06-04 under 510(k) number K031098. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3-CCD DIGITAL CAMERA SYSTEM?

3-CCD DIGITAL CAMERA SYSTEM is a medical device that received FDA 510(k) clearance on 2003-06-04. The listed applicant is Linvatec Corp.. The 510(k) number is K031098.

When did 3-CCD DIGITAL CAMERA SYSTEM receive FDA 510(k) clearance?

3-CCD DIGITAL CAMERA SYSTEM received FDA 510(k) clearance on 2003-06-04, under 510(k) number K031098.

Who is the listed applicant for 3-CCD DIGITAL CAMERA SYSTEM?

The FDA 510(k) record lists Linvatec Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3-CCD DIGITAL CAMERA SYSTEM?

The FDA product code for 3-CCD DIGITAL CAMERA SYSTEM is GCJ.

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Related Devices (Code: GCJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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