Medical Device Manufacturer · US , Walker , MI

Mego Afek - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1981

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Mego Afek Cardiovascular ✕

4 devices

1-4 of 4

Cleared Nov 21, 2007

PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE

Cardiovascular · 90d

Cleared Feb 09, 2006

PBS MODEL 701A COMPRESSION THERAPY DEVICE

Cardiovascular · 10d

Cleared Nov 30, 2001

LYMPHA PRESS PLUS DEVICE

Cardiovascular · 56d

Cleared Oct 20, 1981

Cardiovascular · 253d