LIQUIDERM LIQUID ADHESIVE BANDAGE— 510(k) K002338

Name: FDA 510(k) clearance K002338
Creator: U.S. Food and Drug Administration
Published: 2001-01-29

Substantially Equivalent

Closure Medical Corp.

FDA 510(k) clearance K002338 for LIQUIDERM LIQUID ADHESIVE BANDAGE, Substantially Equivalent on 2001-01-29. Applicant: Closure Medical Corp.. Device class: 1.

Clearance details

Applicant: Closure Medical Corp.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2000-08-01
Decision date: 2001-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raleigh, NC, 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.