Medical Device Manufacturer · US , Port Arthur , TX

Colon Therapeutics - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1984

Recent clearances: JIMMY JOHN III RECTAL NOZZLE, JIMMY JOHN III RECTAL NOZZEL, MODEL CIT

8

Total

8

Cleared

0

Denied

Colon Therapeutics has 8 FDA 510(k) cleared medical devices. Based in Port Arthur, US.

Historical record: 8 cleared submissions from 1984 to 1997. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Colon Therapeutics Filter by specialty or product code using the sidebar.

Colon Therapeutics is one of 14738 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Colon Therapeutics

8 devices

1-8 of 8

Cleared Sep 29, 1997

JIMMY JOHN III RECTAL NOZZLE

Gastroenterology & Urology · 35d

Cleared Sep 09, 1997

JIMMY JOHN III RECTAL NOZZEL, MODEL CIT

Gastroenterology & Urology · 70d

Cleared Jul 20, 1988

Gastroenterology & Urology · 90d

Cleared Oct 14, 1987

MODIFIED RECTAL NOZZLE

Gastroenterology & Urology · 16d

Cleared Mar 17, 1987

MODIFIED JIMMY JOHN III

Gastroenterology & Urology · 67d

Cleared Mar 17, 1987

JIMMY JOHN III, COLONIC IRRIGATION SYSTEM

Gastroenterology & Urology · 47d

Cleared May 15, 1986

JIMMY JOHN III, RECTAL NOZZLE (MODIFICATION)

Gastroenterology & Urology · 64d

Cleared Oct 24, 1984

Gastroenterology & Urology · 154d