COMBIDERM ACD— 510(k) K954918

Name: FDA 510(k) clearance K954918
Creator: U.S. Food and Drug Administration
Published: 1995-12-26

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.. Device class: 1.

Clearance details

Applicant: Convatec, A Bristol-Myers Squibb Co.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1995-10-26
Decision date: 1995-12-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, NJ, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.