Medical Device Manufacturer · US , Solana Beach , CA

Traverse Vascular, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Traverse Vascular, Inc. has 1 FDA 510(k) cleared medical devices. Based in Solana Beach, US.

Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Traverse Vascular, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Traverse Vascular, Inc.

1 devices
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