BIODERM FOAM WOUND DRESSING— 510(k) K973429

Name: FDA 510(k) clearance K973429
Creator: U.S. Food and Drug Administration
Published: 1997-12-01

Substantially Equivalent for Some Indications

Bioderm, Inc.

FDA 510(k) clearance K973429 for BIODERM FOAM WOUND DRESSING, Substantially Equivalent for Some Indications on 1997-12-01. Applicant: Bioderm, Inc.. Device class: 1.

Clearance details

Applicant: Bioderm, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1997-09-10
Decision date: 1997-12-01
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Wheaton, IL, 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.