Arista Medi Prima is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arista Medi Prima - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Arista Medi Prima has 3 FDA 510(k) cleared medical devices. Based in Millbrae, US.
Historical record: 3 cleared submissions from 1996 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Arista Medi Prima Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arista Medi Prima
3 devices