FDA 510(k)

BIOPSY FORCEPS

K-Number: K924106 · 1992-11-24

ApplicantUnited States Endoscopy Group, Inc.

Decision Date1992-11-24

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1992-11-24 under 510(k) number K924106. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPSY FORCEPS?

BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1992-11-24. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K924106.

When did BIOPSY FORCEPS receive FDA 510(k) clearance?

BIOPSY FORCEPS received FDA 510(k) clearance on 1992-11-24, under 510(k) number K924106.

Who is the listed applicant for BIOPSY FORCEPS?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOPSY FORCEPS?

The FDA product code for BIOPSY FORCEPS is KNW.

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Official Source

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