Catheter Research C/O Burditt, Bowles & Radzius
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K924227 | CRI CYNOSAR CATHETER | DRA | 1993-06-29 | View |
| 510(k) | K924125 | CRI ELECTRONIC CONTROL SYSTEM | DXX | 1993-05-26 | View |
| 510(k) | K914523 | CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COIL | DSS | 1992-01-10 | View |
| 510(k) | K904785 | CRI CYNOSAR CATHETER | DRA | 1991-03-06 | View |
| 510(k) | K904787 | CRI STEERABLE CATHETER CONTROL SYSTEM | DXX | 1990-12-17 | View |
| 510(k) | K900320 | CRI CYNOSAR CATHETER | DRA | 1990-09-14 | View |
| 510(k) | K884337 | MICRO-GUIDE SYSTEM | DRA | 1989-01-05 | View |
| 510(k) | K870700 | MICRO-GUIDE | DQO | 1987-12-03 | View |
No matching devices.
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