Codman & Shurtleff, Inc. - FDA 510(k) Cleared Devices
152
Total
151
Cleared
0
Denied
FDA 510(k) cleared devices by Codman & Shurtleff, Inc. Gastroenterology & Urology ✕
5 devices
Cleared
Mar 23, 1993
CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340)
Gastroenterology & Urology
386d
Cleared
Sep 29, 1989
DENVER PERITONEO-VENUS SHUNT
Gastroenterology & Urology
64d
Cleared
Jun 20, 1988
DENVER PLEURO-PERITONEAL SHUNT
Gastroenterology & Urology
131d
Cleared
May 31, 1988
DENVER PERITONEO-VENOUS SHUNT
Gastroenterology & Urology
123d
Cleared
Aug 25, 1987
CODMAN FLEXIBLE ENDOSCOPE
Gastroenterology & Urology
95d