CHESSON LABS LIQUID BANDAGE— 510(k) K083913

Name: FDA 510(k) clearance K083913
Creator: U.S. Food and Drug Administration
Published: 2009-07-31

Substantially Equivalent

Chesson Laboratory Associates, Inc.

FDA 510(k) clearance K083913 for CHESSON LABS LIQUID BANDAGE, Substantially Equivalent on 2009-07-31. Applicant: Chesson Laboratory Associates, Inc.. Device class: 1.

Clearance details

Applicant: Chesson Laboratory Associates, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2008-12-30
Decision date: 2009-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Durham, NC, 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 Chesson Laboratory Associates, Inc.

view all

K120059 — LIQUID BANDAGE2012-05-17

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