Medapp S.A. - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Parexel International as regulatory consultant.
FDA 510(k) Regulatory Record - Medapp S.A.
1 devices