BAND-AID(R) BRAND LIQUID BANDAGE— 510(k) K062602

Name: FDA 510(k) clearance K062602
Creator: U.S. Food and Drug Administration
Published: 2006-12-11

Substantially Equivalent

Johnson & Johnson Consumer Companies, Inc.

FDA 510(k) clearance K062602 for BAND-AID(R) BRAND LIQUID BANDAGE, Substantially Equivalent on 2006-12-11. Applicant: Johnson & Johnson Consumer Companies, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Consumer Companies, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2006-09-01
Decision date: 2006-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skillman, NJ, US

Download summary PDF View on FDA.gov ↗

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