Covidien Lp, Formerly Know AS Valleylab, A Divison
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K110268 | FORCETRIAD ELECTROSURGICAL GENERATOR | GEI | 2011-05-31 | View |
| 510(k) | K072687 | VALLEYLAB MICROWAVE ABLATION GENERATOR | NEY | 2008-11-25 | View |
No matching devices.
Advertisement