Micronica Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Micronica Srl - FDA 510(k) Cleared Devices
Recent clearances: C015
1
Total
1
Cleared
0
Denied
Micronica Srl has 1 FDA 510(k) cleared medical devices. Based in Mirandola, IT.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Micronica Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by THEMA S.r.l. as regulatory consultant.
FDA 510(k) Regulatory Record - Micronica Srl
1 devices