Flaem Nuova S.P.A. is one of 18354 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Flaem Nuova S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: FLAEM NUOVA RF6 BASIC AND RF6 PLUS NEBULIZERS, FAMILIES OF MASTER NEB, PRIMO NEB, SC03, NEB AID, 4.2.NEB, Q03, FJ03, AND WALKIE-NEB
2
Total
2
Cleared
0
Denied
Flaem Nuova S.P.A. has 2 FDA 510(k) cleared medical devices. Based in North Reading, US.
Historical record: 2 cleared submissions from 2007 to 2007. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Flaem Nuova S.P.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Flaem Nuova S.P.A.
2 devices