Medical Device Manufacturer · US , Wayzata , MN

Corvascular Diagnostics, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Corvascular Diagnostics, LLC has 1 FDA 510(k) cleared medical devices. Based in Wayzata, US.

Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Corvascular Diagnostics, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Corvascular Diagnostics, LLC
1 devices
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