Bissell Medical Products, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Advertisement
Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K932880 | GRASSI GASTROJEJUNOSTOMY TUBE | KNT | 1995-06-07 | View |
| 510(k) | K914140 | GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED | FPP | 1992-03-31 | View |
| 510(k) | K901683 | IMPROVED BAKER TWIN-CUFF SUMP TUBE | KNT | 1990-06-27 | View |
| 510(k) | K873441 | BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE | KNT | 1987-10-27 | View |
| 510(k) | K871691 | MODIFIED MULTI-LUMEN NASOGASTRIC TUBE | KNT | 1987-08-10 | View |
| 510(k) | K851672 | NYHUS/NELSON TUBE | KNT | 1985-07-09 | View |
No matching devices.
Advertisement