Bissell Medical Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bissell Medical Products, Inc. Gastroenterology & Urology ✕
5 devices
Cleared
Jun 07, 1995
GRASSI GASTROJEJUNOSTOMY TUBE
Gastroenterology & Urology
723d
Cleared
Jun 27, 1990
IMPROVED BAKER TWIN-CUFF SUMP TUBE
Gastroenterology & Urology
78d
Cleared
Oct 27, 1987
BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE
Gastroenterology & Urology
61d
Cleared
Aug 10, 1987
MODIFIED MULTI-LUMEN NASOGASTRIC TUBE
Gastroenterology & Urology
103d
Cleared
Jul 09, 1985
NYHUS/NELSON TUBE
Gastroenterology & Urology
77d