Medical Device Manufacturer · IL , Kfar Saba

Mego Afek AC , Ltd. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 2008
17
Total
17
Cleared
0
Denied

Mego Afek AC , Ltd. has 17 FDA 510(k) cleared medical devices. Based in Kfar Saba, IL.

Last cleared in 2022. Active since 2008. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Ilan Sharon MD Consultant as regulatory consultant.

FDA 510(k) Regulatory Record - Mego Afek AC , Ltd.

17 devices
1-12 of 17
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