NON-WOVEN COMPRESS— 510(k) K980382

Name: FDA 510(k) clearance K980382
Creator: U.S. Food and Drug Administration
Published: 1998-03-09

Substantially Equivalent for Some Indications

Convatec, A Division of E.R. Squibb & Sons

FDA 510(k) clearance K980382 for NON-WOVEN COMPRESS, Substantially Equivalent for Some Indications on 1998-03-09. Applicant: Convatec, A Division of E.R. Squibb & Sons. Device class: 1.

Clearance details

Applicant: Convatec, A Division of E.R. Squibb & Sons
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1998-02-02
Decision date: 1998-03-09
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Skillman, 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.