# Navarre Biomedical, Ltd.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 9 (1994–1996): 9 510(k) clearances
- Product codes: GBX (5), KRA (1), KGZ (1), FGE (1), EXF (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
- K955110: Navarre Percutaneous Biliary Drainage (Nov 7, 1996)
- K955505: Opti-Drain Multi-Use Drainage Catheter (Feb 7, 1996)
- K945909: Navarre N-Fuser (TM) Peripheral Infusion Catheter (Jun 2, 1995)
- K951907: Navarre Locking Pigtail Universal Drainage Catheter (May 15, 1995)
- K951475: Navarre Universal Drainage Catheter (Apr 24, 1995)
- K943663: Navarre 600 ML Drainage Bag (Sep 8, 1994)
- K942315: Navarre Percutaneous Access Set (Jul 8, 1994)
- K933600: Navarre Biomedical Tip-Locking Drainage Catheters (Mar 28, 1994)

Source page: https://510kreport.com/company/navarre-biomedical