Convatec, A Bristol-Myers Squibb Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Convatec, A Bristol-Myers Squibb Co. - FDA 510(k) Cleared Devices
10
Total
5
Cleared
0
Denied
Convatec, A Bristol-Myers Squibb Co. has 5 FDA 510(k) cleared general & plastic surgery devices. Based in Skillman, US.
Historical record: 5 cleared submissions from 1994 to 2004.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Convatec, A Bristol-Myers Squibb Co.
10 devices
Cleared
Apr 08, 2004
CONVATEC FECAL MANAGEMENT SYSTEM
Gastroenterology & Urology
217d
Cleared
Mar 26, 1999
DUODERM HYDROACTIVE GEL WOUND DRESSING
General & Plastic Surgery
46d
Cleared
Sep 08, 1998
AQUACEL HYDROFIBER WOUND DRESSING
General & Plastic Surgery
84d
Cleared
Dec 29, 1997
DUODERM HYDROACTIVE GEL
General & Plastic Surgery
84d
Cleared
Dec 23, 1997
DUODERM HYDROACTIVE PASTE
General & Plastic Surgery
78d
Cleared
Dec 17, 1997
DUODERM EXTRA THIN CGF DRESSING
General & Plastic Surgery
79d
Cleared
Dec 17, 1997
COMBIDERM ACD
General & Plastic Surgery
79d
Cleared
Dec 26, 1995
COMBIDERM ACD
General & Plastic Surgery
61d
Cleared
Mar 17, 1995
CONQUEST MALE CONTINENCE SYSTEM
Gastroenterology & Urology
268d
Cleared
Nov 22, 1994
EPIVIEW
General & Plastic Surgery
271d