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FDA 510(k)

ZIESS ENDOPROBE

K-Number: K922735 · 1992-07-09

ApplicantCarl Zeiss, Inc.
Decision Date1992-07-09
Product CodeHQB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ZIESS ENDOPROBE 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 1992-07-09 under 510(k) number K922735. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIESS ENDOPROBE?

ZIESS ENDOPROBE is a medical device that received FDA 510(k) clearance on 1992-07-09. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K922735.

When did ZIESS ENDOPROBE receive FDA 510(k) clearance?

ZIESS ENDOPROBE received FDA 510(k) clearance on 1992-07-09, under 510(k) number K922735.

Who is the listed applicant for ZIESS ENDOPROBE?

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 ZIESS ENDOPROBE?

The FDA product code for ZIESS ENDOPROBE is HQB.

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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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