Ferrosan Medical Devices Sp. Z.O.O. is one of 13 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
Recent clearances: Certa Catheter
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.
510(k) submissions have been managed by Ferrosan Medical Devices Sp. Zo.O. C/O Promedic, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ferrosan Medical Devices Sp. Z.O.O.
1 devices