FLEX-AID LIQUID GEL BANDAGE AND DERMAFLEX GEL TISSUE ADHESIVE PROFESSIONAL LIQUID BANDAGE— 510(k) K050757

Name: FDA 510(k) clearance K050757
Creator: U.S. Food and Drug Administration
Published: 2006-02-23

Substantially Equivalent

Chemence Medical, Inc.

FDA 510(k) clearance K050757 for FLEX-AID LIQUID GEL BANDAGE AND DERMAFLEX GEL TISSUE ADHESIVE PROFESSIONAL LIQUID BANDAGE, Substantially Equivalent on 2006-02-23. Applicant: Chemence Medical, Inc.. Device class: 1.

Clearance details

Applicant: Chemence Medical, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2005-03-23
Decision date: 2006-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMF

view all

K241916 — TearRepair Liquid Skin Protectant2024-09-27
K182733 — Rochal Bioshield Silicone Film2019-06-27
K171148 — Aleo BME Liquid Bandage2018-01-12
K153571 — Cavilon Advanced High Endurance Skin Protectant2016-08-23
K160684 — Atteris No-Sting Skin Protectant2016-07-26

More clearances from Chemence Medical, Inc.

view all

K212246 — Exofin Precision Pen2021-09-09
K200264 — Exofin High Viscosity Topical Skin Adhesive2020-12-17
K191461 — Exofin Fusion Skin Closure System2020-06-05
K171442 — Exofin Fusion Skin Closure System2017-09-25
K162352 — derma+flex QS High Viscosity Tissue Adhesive2016-12-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.