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FDA 510(k)

SKIN STAPLING INSTRUMENT

K-Number: K760732 · 1976-11-03

ApplicantETHICON, Inc.
Decision Date1976-11-03
Product CodeGAG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SKIN STAPLING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1976-11-03 under 510(k) number K760732. The device is classified under product code GAG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIN STAPLING INSTRUMENT?

SKIN STAPLING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1976-11-03. The listed applicant is ETHICON, Inc.. The 510(k) number is K760732.

When did SKIN STAPLING INSTRUMENT receive FDA 510(k) clearance?

SKIN STAPLING INSTRUMENT received FDA 510(k) clearance on 1976-11-03, under 510(k) number K760732.

Who is the listed applicant for SKIN STAPLING INSTRUMENT?

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

What is the FDA product code for SKIN STAPLING INSTRUMENT?

The FDA product code for SKIN STAPLING INSTRUMENT is GAG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing ETHICON, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 195 devices →

Related Devices (Code: GAG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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