Merivaara Instrumentarium Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Merivaara Instrumentarium Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Merivaara Instrumentarium Corp. has 4 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.
Historical record: 4 cleared submissions from 1994 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Merivaara Instrumentarium Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Merivaara Instrumentarium Corp.
4 devices