510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940895Substantially Equivalent for Some Indications

Epiview

Convatec, A Bristol-Myers Squibb Co., Skillman NJ / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K940895 is the FDA 510(k) clearance record for EPIVIEW, cleared for Convatec, A Bristol-Myers Squibb Co. on under FDA product code MGP (Dressing, Wound And Burn, Occlusive). FDA records list 10 510(k) clearances for Convatec, A Bristol-Myers Squibb Co., from to . As of , FDA records show no recalls naming K940895.

Clearance record

Decision date
Received
(271 days to decision)
Product code
MGP Dressing, Wound And Burn, Occlusive
Device class
Unclassified
Review panel
Unknown
Applicant
Convatec, A Bristol-Myers Squibb Co. 200 Headquarters Park Dr., Skillman NJ
Third party review
No

Clearances, product code MGP

Trailing 12 months

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

FDA records show no clearances under product code MGP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MGP, 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