Medical Device Manufacturer · US , Mchenry , IL

Norwich Eaton Pharmaceuticals, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1980

10

Total

10

Cleared

0

Denied

Norwich Eaton Pharmaceuticals, Inc. has 10 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1980 to 1984.

Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Norwich Eaton Pharmaceuticals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Norwich Eaton Pharmaceuticals, Inc.

10 devices

1-10 of 10

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 Sep 07, 1982

VIVONEX MASS GASTRASTOMY TUBE

Immunology · 18d

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