# Catheter Technology Corp.

- Location (FDA's records): Walker, MI
- FDA decisions: 13 (1983–1988): 13 510(k) clearances
- Product codes: FOZ (2), JHJ (2), LJS (2), FGE (1), DQY (1), FOS (1), GTQ (1), DCN (1), LKS (1), LJT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Catheter Innovations, Inc.: 2 (https://510kreport.com/company/catheter-innovations)
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K880571: Cath-Tech Port Implantable Vascular Access System (1988), cited by 4

## Recent decisions
- K880571: Cath-Tech Port Implantable Vascular Access System (Mar 4, 1988)
- K871080: Peripherally Inserted Central Venous Catheter (Aug 12, 1987)
- K871998: Groshong CV Catheter Repair Kit (Jun 24, 1987)
- K860256: Brawn and Groshong Catheters (Mar 28, 1986)
- K842577: Cath-Tech Polyurethane Umbilical Vess (Mar 13, 1985)
- K842147: Cath-Tech Cholangiography Catheter (Oct 2, 1984)
- K840339: Umbilical Vessel Catheter (Jul 25, 1984)
- K831386: Groshong Catheter, Long Term Type (Oct 14, 1983)

Source page: https://510kreport.com/company/catheter-technology