Medinet Srl is one of 222 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Medinet Srl - FDA 510(k) Cleared Devices
Recent clearances: MEDINET INCENTIVE SPIROMETERS - RESPIPROGRAM
1
Total
1
Cleared
0
Denied
Medinet Srl has 1 FDA 510(k) cleared medical devices. Based in Milano, IT.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medinet Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Isemed S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - Medinet Srl
1 devices