Bissell Medical Products, Inc.
Bissell Medical Products, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 7, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K932880 | GRASSI GASTROJEJUNOSTOMY TUBE | June 7, 1995 |
| K914140 | GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED | March 31, 1992 |
| K901683 | IMPROVED BAKER TWIN-CUFF SUMP TUBE | June 27, 1990 |
| K873441 | BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE | October 27, 1987 |
| K871691 | MODIFIED MULTI-LUMEN NASOGASTRIC TUBE | August 10, 1987 |
| K851672 | NYHUS/NELSON TUBE | July 9, 1985 |