Catheter Research C/O Burditt, Bowles & Radzius
Catheter Research C/O Burditt, Bowles & Radzius appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 29, 1993.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K924227 | CRI CYNOSAR CATHETER | June 29, 1993 |
| K924125 | CRI ELECTRONIC CONTROL SYSTEM | May 26, 1993 |
| K914523 | CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COIL | January 10, 1992 |
| K904785 | CRI CYNOSAR CATHETER | March 6, 1991 |
| K904787 | CRI STEERABLE CATHETER CONTROL SYSTEM | December 17, 1990 |
| K900320 | CRI CYNOSAR CATHETER | September 14, 1990 |
| K884337 | MICRO-GUIDE SYSTEM | January 5, 1989 |
| K870700 | MICRO-GUIDE | December 3, 1987 |