Colon Therapeutics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Colon Therapeutics - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Colon Therapeutics
8 devices
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
JIMMY JOHN III
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
JIMMY JOHN III
Gastroenterology & Urology
154d