Company ยท US
Bissell Medical Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1995. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 7, 1995 | K932880 | GRASSI GASTROJEJUNOSTOMY TUBE Bissell Medical Products, Inc. | KNT |
| Mar 31, 1992 | K914140 | GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED Bissell Medical Products, Inc. | FPP |
| Jun 27, 1990 | K901683 | IMPROVED BAKER TWIN-CUFF SUMP TUBE Bissell Medical Products, Inc. | KNT |
| Oct 27, 1987 | K873441 | BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE Bissell Medical Products, Inc. | KNT |
| Aug 10, 1987 | K871691 | MODIFIED MULTI-LUMEN NASOGASTRIC TUBE Bissell Medical Products, Inc. | KNT |
| Jul 9, 1985 | K851672 | NYHUS/NELSON TUBE Bissell Medical Products, Inc. | KNT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||