Osprey Medical, Inc. - FDA 510(k) Cleared Devices

Osprey Medical, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Eden Prairie, US.

Historical record: 14 cleared submissions from 2013 to 2019.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant. 2 devices have linked clinical trials registered on ClinicalTrials.gov.