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

Mego Afek has 5 FDA 510(k) cleared medical devices. Based in Walker, US.

Last cleared in 2023. Active since 1981. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Mego Afek Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mego Afek

5 devices

1-5 of 5

Cleared Apr 04, 2023

Ballancer Platinum (1222)

Physical Medicine · 49d

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