FDA 510(k) Applications Submitted by MEGO AFEK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072372 | 08/23/2007 | PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE | MEGO AFEK |
| K013331 | 10/05/2001 | LYMPHA PRESS PLUS DEVICE | MEGO AFEK |
| K060220 | 01/30/2006 | PBS MODEL 701A COMPRESSION THERAPY DEVICE | MEGO AFEK |
| K230385 | 02/14/2023 | Ballancer Platinum (1222) | Mego Afek |
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