510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901877Substantially Equivalent

Allevyn Dressing (Labeling Revised)

Smith & Nephew United, Inc., Largo FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901877 is the FDA 510(k) clearance record for ALLEVYN DRESSING (LABELING REVISED), a class I device, cleared for Smith & Nephew United, Inc. on under FDA product code KMF (Bandage, Liquid). FDA records list 34 510(k) clearances for Smith & Nephew United, Inc., from to . As of , FDA records show no recalls naming K901877.

Clearance record

Decision date
Received
(57 days to decision)
Product code
KMF Bandage, Liquid
Regulation
21 CFR 880.5090
Device class
Class I
Review panel
General Hospital
Applicant
Smith & Nephew United, Inc. 11775 Starkley Rd., Largo FL
Third party review
No

Clearances, product code KMF

Trailing 12 months

FDA records hold no clearances under product code KMF in the trailing twelve months.

FDA records show no clearances under product code KMF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KMF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260