Corpak Co. - FDA 510(k) Cleared Devices
21
Total
20
Cleared
0
Denied
Corpak Co. has 20 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1981 to 1996. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Corpak Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Corpak Co.
21 devices
Cleared
Aug 29, 1996
CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE
Gastroenterology & Urology
1017d
Cleared
Jun 09, 1995
CORPAK GASTROSTOMY TUBE
Gastroenterology & Urology
784d
Cleared
Jun 17, 1994
CORPAK ENTERAL PUMP
General Hospital
372d
Cleared
Aug 30, 1990
CORPAK GRASPING FORCEPS
Gastroenterology & Urology
56d
Cleared
Jun 11, 1990
CORPAK GASTROSTOMY TUBE
Gastroenterology & Urology
73d
Cleared
Sep 21, 1988
CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE
Gastroenterology & Urology
72d
Cleared
Nov 05, 1985
CORPAK FARRELL VALVE ENTERAL GASTRIC PRESSURE RELI
Gastroenterology & Urology
95d
Cleared
Aug 08, 1985
CORPAK ENTERAL SOL ADM PUMP SET W/ SCREW
Gastroenterology & Urology
38d
Cleared
Aug 08, 1984
CORPAK URINARY DRAINAGE BAG
Gastroenterology & Urology
62d
Cleared
Jul 19, 1984
CORPAK FOLEY CATH TRAY W/16FR. TEFLON
Gastroenterology & Urology
78d
Cleared
Mar 16, 1984
URETHRAL CATH. TRAY W/BAG
Gastroenterology & Urology
52d
Cleared
Aug 16, 1983
CORPAK VTR 300 ENTERNAL PUMP
General Hospital
42d