# Bissell Medical Products, Inc.

- Location (FDA's records): Naperville, IL
- FDA decisions: 6 (1985–1995): 6 510(k) clearances
- Product codes: KNT (5), FPP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K932880: Grassi Gastrojejunostomy Tube (Jun 7, 1995)
- K914140: Grassi Gastrojejun Tube Gastric Decomp/Jejun Feed (Mar 31, 1992)
- K901683: Improved Baker Twin-Cuff Sump Tube (Jun 27, 1990)
- K873441: Baker Twin-Cuff Intestinal Decomp/Plication Tube (Oct 27, 1987)
- K871691: Modified Multi-Lumen Nasogastric Tube (Aug 10, 1987)
- K851672: Nyhus/Nelson Tube (Jul 9, 1985)

Source page: https://510kreport.com/company/bissell-medical-products