Mego Afek - FDA 510(k) Cleared Devices
Recent clearances: Ballancer Platinum (1222), PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE, PBS MODEL 701A COMPRESSION THERAPY DEVICE
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mego Afek Cardiovascular ✕
4 devices