ACRYDERM ADVANCED WOUND DRESSING— 510(k) K943781

Name: FDA 510(k) clearance K943781
Creator: U.S. Food and Drug Administration
Published: 1994-10-04

Substantially Equivalent for Some Indications

Acrymed, Inc.

FDA 510(k) clearance K943781 for ACRYDERM ADVANCED WOUND DRESSING, Substantially Equivalent for Some Indications on 1994-10-04. Applicant: Acrymed, Inc.. Device class: 1.

Clearance details

Applicant: Acrymed, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1994-08-03
Decision date: 1994-10-04
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Lake Oswego, OR, 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.