FDA 510(k)

BIOPLAR FORCEPS

K-Number: K943231 · 1994-07-26

Decision Date1994-07-26

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BIOPLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Cook Urological, Inc.. It received FDA 510(k) clearance on 1994-07-26 under 510(k) number K943231. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPLAR FORCEPS?

BIOPLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1994-07-26. The listed applicant is Cook Urological, Inc.. The 510(k) number is K943231.

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

BIOPLAR FORCEPS received FDA 510(k) clearance on 1994-07-26, under 510(k) number K943231.

Who is the listed applicant for BIOPLAR FORCEPS?

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

What is the FDA product code for BIOPLAR FORCEPS?

The FDA product code for BIOPLAR FORCEPS is GEI.

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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.