KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE— 510(k) K131384

Name: FDA 510(k) clearance K131384
Creator: U.S. Food and Drug Administration
Published: 2014-08-07

Substantially Equivalent

Kericure, Inc.

FDA 510(k) clearance K131384 for KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE, Substantially Equivalent on 2014-08-07. Applicant: Kericure, Inc.. Device class: 1.

Clearance details

Applicant: Kericure, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2013-05-14
Decision date: 2014-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Apollo Beach, FL, 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.