12
Total
12
Cleared
0
Denied

Trireme Medical, Inc. has 12 FDA 510(k) cleared cardiovascular devices. Based in Pleasanton, US.

Historical record: 12 cleared submissions from 2010 to 2014.

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

Regulatory submissions have been managed by Intertek Testing Services, Citech and Regulatory Technology Services, LLC.

FDA 510(k) Regulatory Record - Trireme Medical, Inc.

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