Covidien, LLC, Formerly Registered AS Tyco Healthca
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K102605 | MAHURKAR TRIPLE LUMEN DIALYSIS CATHETER | NIE | 2010-12-22 | View |
| 510(k) | K102325 | IDRIVE SYSTEM (I DRIVE POWER HANDLE, IDRIVE (RALC) SINGLE USE RELOAD) | GDW | 2010-10-13 | View |
No matching devices.
Advertisement