FDA 510(k)

STIEGMANN-GOFF ENDOSCOPIC LIGATOR

K-Number: K940661 · 1994-11-28

Decision Date1994-11-28

Product CodeMND

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

STIEGMANN-GOFF ENDOSCOPIC LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1994-11-28 under 510(k) number K940661. The device is classified under product code MND. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIEGMANN-GOFF ENDOSCOPIC LIGATOR?

STIEGMANN-GOFF ENDOSCOPIC LIGATOR is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K940661.

When did STIEGMANN-GOFF ENDOSCOPIC LIGATOR receive FDA 510(k) clearance?

STIEGMANN-GOFF ENDOSCOPIC LIGATOR received FDA 510(k) clearance on 1994-11-28, under 510(k) number K940661.

Who is the listed applicant for STIEGMANN-GOFF ENDOSCOPIC LIGATOR?

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

What is the FDA product code for STIEGMANN-GOFF ENDOSCOPIC LIGATOR?

The FDA product code for STIEGMANN-GOFF ENDOSCOPIC LIGATOR is MND.

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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.