Percu Surge, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K003992 | PERCUSURGE GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM | NFA | 2001-06-01 | View |
| 510(k) | K972777 | TEMPORARY OCCLUSION BALLOON SYSTEM | MJN | 1998-03-11 | View |
No matching devices.
Advertisement