510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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KMFClass I

Bandage, Liquid

21 CFR 880.5090 / General Hospital
FDA source (opens on fda.gov)

KMF is the FDA product code for Bandage, Liquid, a class I device type, regulated under 21 CFR 880.5090. As of , FDA records hold 222 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
KMF
Device name
Bandage, Liquid
Regulation
21 CFR 880.5090
Device class
Class I
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
222
Ingested recalls
4

Clearances, product code KMF

By decision year
222 clearances under product code KMF with a decision year between 1977 and 2024, 1994 the highest year at 32.
Show the numbers
510(k) clearances under FDA product code KMF by decision year
YearClearances
19771
19784
19793
19801
19813
19821
19841
19861
19892
19907
19913
199214
199316
199432
199532
199617
199718
199822
199912
20001
20012
20021
20033
20043
20051
20064
20072
20083
20093
20101
20121
20142
20162
20181
20191
20241

Applicants with the most clearances

Product code KMF
Applicants holding the most 510(k) clearances under product code KMF
ApplicantClearances
Convatec, A Division of E.R. Squibb & Sons13
Kendall Healthcare Products Co. Div.Of Tyco Health9
Bioderm, Inc.7
MEDLINE INDUSTRIES, LP - Northfield7
Smith & Nephew United, Inc.7
Innovative Technologies, Ltd.6
3M Company5
Acme United Corp.5
Derma Sciences, Inc.5
Ferris Mfg. Corp.5

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 66 companies shown, in name order