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FDA 510(k)

BABCOCK/BOWEL CLAMP FORCEPS

K-Number: K940790 · 1994-11-03

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1994-11-03
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BABCOCK/BOWEL CLAMP FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1994-11-03 under 510(k) number K940790. 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 BABCOCK/BOWEL CLAMP FORCEPS?

BABCOCK/BOWEL CLAMP FORCEPS is a medical device that received FDA 510(k) clearance on 1994-11-03. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K940790.

When did BABCOCK/BOWEL CLAMP FORCEPS receive FDA 510(k) clearance?

BABCOCK/BOWEL CLAMP FORCEPS received FDA 510(k) clearance on 1994-11-03, under 510(k) number K940790.

Who is the listed applicant for BABCOCK/BOWEL CLAMP FORCEPS?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BABCOCK/BOWEL CLAMP FORCEPS?

The FDA product code for BABCOCK/BOWEL CLAMP FORCEPS 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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