ALLKARE BARRIER WIPE— 510(k) K925004

Name: FDA 510(k) clearance K925004
Creator: U.S. Food and Drug Administration
Published: 1994-01-12

Substantially Equivalent

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

FDA 510(k) clearance K925004 for ALLKARE BARRIER WIPE, Substantially Equivalent on 1994-01-12. 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: 1992-10-02
Decision date: 1994-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, 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.