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FDA 510(k)

XENON ARC ENDOSCOPE LIGHT SOURCE

K-Number: K920403 · 1992-02-21

ApplicantMedical Device Inspection Co., Inc.
Decision Date1992-02-21
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

XENON ARC ENDOSCOPE LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1992-02-21 under 510(k) number K920403. 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 XENON ARC ENDOSCOPE LIGHT SOURCE?

XENON ARC ENDOSCOPE LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1992-02-21. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K920403.

When did XENON ARC ENDOSCOPE LIGHT SOURCE receive FDA 510(k) clearance?

XENON ARC ENDOSCOPE LIGHT SOURCE received FDA 510(k) clearance on 1992-02-21, under 510(k) number K920403.

Who is the listed applicant for XENON ARC ENDOSCOPE LIGHT SOURCE?

The FDA 510(k) record lists Medical Device Inspection Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XENON ARC ENDOSCOPE LIGHT SOURCE?

The FDA product code for XENON ARC ENDOSCOPE LIGHT SOURCE is 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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