Medical Device Manufacturer · US , Danvers , MA

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

1 submissions · 1 cleared · Since 2026

Total

Cleared

Denied

Medtronic Interventional Vascular, Inc. has 1 FDA 510(k) cleared medical devices. Based in Danvers, US.

Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Cardiovascular.

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

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

1 devices

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