Bissell Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bissell Medical Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Bissell Medical Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 6 cleared submissions from 1985 to 1995. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Bissell Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bissell Medical Products, Inc.
6 devices
Cleared
Jun 07, 1995
GRASSI GASTROJEJUNOSTOMY TUBE
Gastroenterology & Urology
723d
Cleared
Mar 31, 1992
GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED
General Hospital
197d
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