# Med Institute, Inc.

- Location (FDA's records): West Lafayette, IN
- FDA decisions: 26 (1990–2000): 26 510(k) clearances
- Product codes: LJT (17), DRE (2), GCC (2), DWF (1), MQR (1), KNT (1), FMI (1), ITX (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cook Pacemaker Corp.: 1 (https://510kreport.com/company/cook-pacemaker)

## Firms that cite its devices most
- Cook Vascular, Inc.: 1 (https://510kreport.com/company/cook-vascular)
- Wilson-Cook Medical, Inc.: 1 (https://510kreport.com/company/wilson-cook-medical)

## Its most-cited devices
- K990034: Wilson-Cook Colonic Z-Stent (2000), cited by 1
- K945586: Flexible Dilating Sheath (1997), cited by 1
- K964001: Swartz Doppler Flow Probe and Monitor System (1998), cited by 1

## Recent decisions
- K990034: Wilson-Cook Colonic Z-Stent (Apr 17, 2000)
- K982507: Mini Polyurethane Catheter (Sep 16, 1998)
- K981061: Intravascular Retrieval Device (May 26, 1998)
- K964001: Swartz Doppler Flow Probe and Monitor System (Apr 17, 1998)
- K971140: Vital-Port Infusion Pal (Nov 17, 1997)
- K970442: Target Vital-Port Vascular Access System (Apr 30, 1997)
- K945586: Flexible Dilating Sheath (Apr 4, 1997)
- K960698: Non-Coring Needle (Apr 15, 1996)

Source page: https://510kreport.com/company/med-institute