Mego Afek
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K230385 | Ballancer Platinum (1222) | IRP | 2023-04-04 | View |
| 510(k) | K072372 | PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE | JOW | 2007-11-21 | View |
| 510(k) | K060220 | PBS MODEL 701A COMPRESSION THERAPY DEVICE | JOW | 2006-02-09 | View |
| 510(k) | K013331 | LYMPHA PRESS PLUS DEVICE | JOW | 2001-11-30 | View |
| 510(k) | K810338 | LYMPHA PRESS | JOW | 1981-10-20 | View |
No matching devices.
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