COMBIDERM ACD— 510(k) K954918

Substantially Equivalent

Convatec, A Bristol-Myers Squibb Co.

FDA 510(k) clearance K954918 for COMBIDERM ACD, Substantially Equivalent on 1995-12-26. Applicant: Convatec, A Bristol-Myers Squibb Co..

Clearance details

Applicant: Convatec, A Bristol-Myers Squibb Co.
Product code: Code KMF
Advisory panel: General Hospital
Date received: 1995-10-26
Decision date: 1995-12-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, NJ, US

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