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FDA 510(k)

ZEISS ENDOLIVE STERO ENDOSCOPE

K-Number: K950985 · 1995-03-29

ApplicantCarl Zeiss, Inc.
Decision Date1995-03-29
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ZEISS ENDOLIVE STERO ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss, Inc.. It received FDA 510(k) clearance on 1995-03-29 under 510(k) number K950985. 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 ZEISS ENDOLIVE STERO ENDOSCOPE?

ZEISS ENDOLIVE STERO ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1995-03-29. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K950985.

When did ZEISS ENDOLIVE STERO ENDOSCOPE receive FDA 510(k) clearance?

ZEISS ENDOLIVE STERO ENDOSCOPE received FDA 510(k) clearance on 1995-03-29, under 510(k) number K950985.

Who is the listed applicant for ZEISS ENDOLIVE STERO ENDOSCOPE?

The FDA 510(k) record lists Carl Zeiss, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZEISS ENDOLIVE STERO ENDOSCOPE?

The FDA product code for ZEISS ENDOLIVE STERO ENDOSCOPE is GCJ.

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Other records listing Carl Zeiss, Inc. as applicant

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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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