FDA 510(k)

HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR

K-Number: K955120 · 1996-01-26

Decision Date1996-01-26

Product CodeGCM

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 1996-01-26 under 510(k) number K955120. The device is classified under product code GCM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR?

HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR is a medical device that received FDA 510(k) clearance on 1996-01-26. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K955120.

When did HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR receive FDA 510(k) clearance?

HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR received FDA 510(k) clearance on 1996-01-26, under 510(k) number K955120.

Who is the listed applicant for HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR?

The FDA 510(k) record lists Ethicon Endo-Surgery, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR?

The FDA product code for HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR is GCM.

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Other records listing Ethicon Endo-Surgery, Inc. as applicant

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Related Devices (Code: GCM)

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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.