Norwich Eaton Pharmaceuticals, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Norwich Eaton Pharmaceuticals, Inc. Gastroenterology & Urology ✕
9 devices
Cleared
Aug 14, 1984
VIVONEX TUNG STEN TIP TUBE
Gastroenterology & Urology
25d
Cleared
Sep 01, 1983
VIVONEX TUNGSTEN TIP TUBE-BRAIDED
Gastroenterology & Urology
73d
Cleared
Sep 01, 1983
VIVONEX TUNGSTEN TIP TUBE-WOUND
Gastroenterology & Urology
73d
Cleared
Sep 01, 1983
VIVONEX TUNGSTEN TIP TUBE-TWISTED WIRE
Gastroenterology & Urology
73d
Cleared
Jul 18, 1983
VIVONEX TUNGSTEN TIP TUBE-MONOFILA-
Gastroenterology & Urology
28d
Cleared
May 10, 1982
VIVONEX TUNGSTEN TIP TUBE PLACEMENT
Gastroenterology & Urology
13d
Cleared
Apr 29, 1982
VIVONEX ACUTROL ENTERNAL FEEDING SYS
Gastroenterology & Urology
13d
Cleared
Aug 25, 1981
VIVONEX TUNGSTEN TIP
Gastroenterology & Urology
46d
Cleared
Oct 23, 1980
VIVONEX JEJUNOSTOMY KIT
Gastroenterology & Urology
31d