# Catheter Research C/O Burditt, Bowles & Radzius

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 8 (1987–1993): 8 510(k) clearances
- Product codes: DRA (4), DXX (2), DSS (1), DQO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Velocimed, Inc.: 1 (https://510kreport.com/company/velocimed)
- Baxter Edwards: 1 (https://510kreport.com/company/baxter-edwards)
- Stereotaxis, Inc.: 1 (https://510kreport.com/company/stereotaxis)

## Its most-cited devices
- K914523: Cri Vessel Occlusin System/Cri Occlusion Coil (1992), cited by 1
- K924125: Cri Electronic Control System (1993), cited by 1
- K904785: Cri Cynosar Catheter (1991), cited by 1

## Recent decisions
- K924227: Cri Cynosar Catheter (Jun 29, 1993)
- K924125: Cri Electronic Control System (May 26, 1993)
- K914523: Cri Vessel Occlusin System/Cri Occlusion Coil (Jan 10, 1992)
- K904785: Cri Cynosar Catheter (Mar 6, 1991)
- K904787: Cri Steerable Catheter Control System (Dec 17, 1990)
- K900320: Cri Cynosar Catheter (Sep 14, 1990)
- K884337: Micro-Guide System (Jan 5, 1989)
- K870700: Micro-Guide (Dec 3, 1987)

Source page: https://510kreport.com/company/catheter-research-c-o-burditt-bowles-radzius