Home / 510(k) Clearances / K120059

510(k) K120059

LIQUID BANDAGE by Chesson Laboratory Associates, Inc. — Product Code KMF

K120059 is an FDA 510(k) premarket notification submitted by Chesson Laboratory Associates, Inc. for the device "LIQUID BANDAGE". The FDA issued a decision of Substantially Equivalent on May 17, 2012. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Chesson Laboratory Associates, Inc. has at least 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 17, 2012
Date Received
January 9, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Liquid
Device Class
Class I
Regulation Number
880.5090
Review Panel
SU
Submission Type

Other clearances by Chesson Laboratory Associates, Inc.

  • K083913 — CHESSON LABS LIQUID BANDAGE (July 31, 2009)

Other clearances for product code KMF

  • K241916 — TearRepair Liquid Skin Protectant (September 27, 2024)
  • K182733 — Rochal Bioshield Silicone Film (June 27, 2019)
  • K171148 — Aleo BME Liquid Bandage (January 12, 2018)
  • K153571 — Cavilon Advanced High Endurance Skin Protectant (August 23, 2016)
  • K160684 — Atteris No-Sting Skin Protectant (July 26, 2016)
  • K131384 — KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE (August 7, 2014)
  • K133443 — MARATHON NO STING LIQUID SKIN PROTECTANT (July 10, 2014)
  • K092712 — SKIN BARRIER FILM (February 23, 2010)
  • K083087 — ECOCEL (August 7, 2009)
  • K083913 — CHESSON LABS LIQUID BANDAGE (July 31, 2009)

FDA data resources