ALLKARE(TM) ADHESIVE REMOVER WIPE— 510(k) K924976

Name: FDA 510(k) clearance K924976
Creator: U.S. Food and Drug Administration
Published: 1993-04-20

Substantially Equivalent

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

FDA 510(k) clearance K924976 for ALLKARE(TM) ADHESIVE REMOVER WIPE, Substantially Equivalent on 1993-04-20. 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 KOX
Device class: Class 1
Regulation: 21 CFR 878.4730
Advisory panel: General, Plastic Surgery
Date received: 1992-10-01
Decision date: 1993-04-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, NJ, US

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K925618 — 3M REMOVER LOTION PRODUCT NUMBER 86XX1993-03-31
K923351 — SKIN SUPPORT PREP PAD1992-09-14

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K980720 — NONWOVEN PAD1998-04-15
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Data sourced from openFDA. This site is unofficial and independent of the FDA.