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FDA 510(k) K142122, RADAR VASCULAR COMPRESSION DEVICE, by Advanced Vascular Dynamics

FDA 510(k) K142122, RADAR VASCULAR COMPRESSION DEVICE, by Advanced Vascular Dynamics

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510(K) Number: K142122
Device Name: RADAR VASCULAR COMPRESSION DEVICE
Manufacturer: Advanced Vascular Dynamics
Device Classification Name: clamp, vascular
Regulation Number: 870.4450
Classification Product Code: DXC
Date Received: 08/04/2014
Decision Date: 12/04/2014
Regulation Medical Specialty: Cardiovascular
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