Medical Device Manufacturer · US , Grand Rapids , MI

Surge Cardiovascular - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Surge Cardiovascular has 1 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Surge Cardiovascular Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Surge Cardiovascular

1 devices

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