Medical Device Manufacturer · PL , Krakow

Medapp S.A. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

1

Total

1

Cleared

0

Denied

Medapp S.A. has 1 FDA 510(k) cleared medical devices. Based in Krakow, PL.

Last cleared in 2023. Active since 2023. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Medapp S.A. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Medapp S.A.

1 devices

1-1 of 1

Cleared May 01, 2023

Radiology · 307d