Merit Cro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Merit Cro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Excelsior
1
Total
1
Cleared
0
Denied
Merit Cro, Inc. has 1 FDA 510(k) cleared medical devices. Based in Madison, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Merit Cro, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O'Connell Regulatory Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Merit Cro, Inc.
1 devices