MEPITEL NON-ADHERENT SILICONE DRESSING— 510(k) K914604

Name: FDA 510(k) clearance K914604
Creator: U.S. Food and Drug Administration
Published: 1992-03-25

Substantially Equivalent

Molnlycke Clinical Products AB

FDA 510(k) clearance K914604 for MEPITEL NON-ADHERENT SILICONE DRESSING, Substantially Equivalent on 1992-03-25. Applicant: Molnlycke Clinical Products AB. Device class: 1.

Clearance details

Applicant: Molnlycke Clinical Products AB
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1991-10-17
Decision date: 1992-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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