FDA 510(k)

APPOSE SKIN STAPLER & REMOVER

K-Number: K823552 · 1983-06-15

Decision Date1983-06-15

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

APPOSE SKIN STAPLER & REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is American Cyanamid Co.. It received FDA 510(k) clearance on 1983-06-15 under 510(k) number K823552. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APPOSE SKIN STAPLER & REMOVER?

APPOSE SKIN STAPLER & REMOVER is a medical device that received FDA 510(k) clearance on 1983-06-15. The listed applicant is American Cyanamid Co.. The 510(k) number is K823552.

When did APPOSE SKIN STAPLER & REMOVER receive FDA 510(k) clearance?

APPOSE SKIN STAPLER & REMOVER received FDA 510(k) clearance on 1983-06-15, under 510(k) number K823552.

Who is the listed applicant for APPOSE SKIN STAPLER & REMOVER?

The FDA 510(k) record lists American Cyanamid Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APPOSE SKIN STAPLER & REMOVER?

The FDA product code for APPOSE SKIN STAPLER & REMOVER is GDW.

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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.