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FDA 510(k), K092503, RADAR VASCULAR COMPRESSION DEVICES
FDA 510(k), K092503, RADAR VASCULAR COMPRESSION DEVICES
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510(K) Number: K092503
Device Name: RADAR VASCULAR COMPRESSION DEVICES
Manufacturer: MATTHEW SEMLER
Device Classification Name: Clamp, Vascular
Regulation Number: DXC
Classification Product Code: 08/14/2009
Date Received: 11/19/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: RADAR VASCULAR COMPRESSION DEVICES
Manufacturer: MATTHEW SEMLER
Device Classification Name: Clamp, Vascular
Regulation Number: DXC
Classification Product Code: 08/14/2009
Date Received: 11/19/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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