Medi USA, LP
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2022-07-07
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221654 | medi pneumatic compression system (pcs)-genius (Model 652) | JOW | 2022-07-07 | View |
| 510(k) | K183631 | medi pneumatic compression system (pcs) – brio (Model 651) | JOW | 2019-01-25 | View |
No matching devices.