Ferrosan Medical Devices Sp. Z.O.O. is one of 10 FDA 510(k) medical device manufacturers from Poland in the dataset, ranked by real submission volume.
Ferrosan Medical Devices Sp. Z.O.O. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ferrosan Medical Devices Sp. Z.O.O. has 1 FDA 510(k) cleared medical devices. Based in Szczecin, PL.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Ferrosan Medical Devices Sp. Z.O.O. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ferrosan Medical Devices Sp. Z.O.O.
1 devices