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KMF — Bandage, Liquid Class I

FDA Device Classification

Classification Details

Product Code
KMF
Device Class
Class I
Regulation Number
880.5090
Submission Type
Review Panel
SU
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K241916optmedTearRepair Liquid Skin ProtectantSeptember 27, 2024
K182733rochal industriesRochal Bioshield Silicone FilmJune 27, 2019
K171148aleo bmeAleo BME Liquid BandageJanuary 12, 2018
K1535713m healthcareCavilon Advanced High Endurance Skin ProtectantAugust 23, 2016
K160684rochal industriesAtteris No-Sting Skin ProtectantJuly 26, 2016
K131384kericureKERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGEAugust 7, 2014
K133443advanced medical solutions (plymouth)MARATHON NO STING LIQUID SKIN PROTECTANTJuly 10, 2014
K120059chesson laboratory associatesLIQUID BANDAGEMay 17, 2012
K092712lodestar productsSKIN BARRIER FILMFebruary 23, 2010
K083087polichemECOCELAugust 7, 2009
K083913chesson laboratory associatesCHESSON LABS LIQUID BANDAGEJuly 31, 2009
K083752glustitchGLUSEAL 90, MODEL GLU9010February 23, 2009
K082703marine polymer technologiesMRDH BANDAGEOctober 14, 2008
K081009novabay pharmaceuticalsNEUTROPHASEMay 20, 2008
K073663biocureGELSPRAY WOUND DRESSINGJanuary 30, 2008
K063202procurement technology systemsPRODERMA LIQUID BANDAGEMay 2, 2007
K984207argentum internationalSILVERLON DIRECT PRESSURE WOUND DRESSINGMarch 19, 2007
K062602johnson and johnson consumer companiesBAND-AID(R) BRAND LIQUID BANDAGEDecember 11, 2006
K0534093m3M LIQUID BANDAGEJune 19, 2006
K042955d and d holdingsCUTICOVER SKIN BARRIER DEVICEJune 19, 2006