Medical Device Manufacturer · US , White Bear Lake , MN

Neurovena Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

Total

Cleared

Denied

Neurovena Corp. has 1 FDA 510(k) cleared medical devices. Based in White Bear Lake, US.

Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Cardiovascular.

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

Neurovena Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neurovena Corp.

1 devices

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