DERMAGRAN WOUND MANAGEMENT SYSTEM— 510(k) K970660

Name: FDA 510(k) clearance K970660
Creator: U.S. Food and Drug Administration
Published: 1997-08-12

Substantially Equivalent

Derma Sciences, Inc.

FDA 510(k) clearance K970660 for DERMAGRAN WOUND MANAGEMENT SYSTEM, Substantially Equivalent on 1997-08-12. Applicant: Derma Sciences, Inc.. Device class: 1.

Clearance details

Applicant: Derma Sciences, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1997-02-21
Decision date: 1997-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, 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.