FDA 510(k), K093397, TRAXCESS 14EX GUIDEWIRE AND TRAXCESS DOCKING WIRE
FDA 510(k), K093397, TRAXCESS 14EX GUIDEWIRE AND TRAXCESS DOCKING WIRE
Device Name: TRAXCESS 14EX GUIDEWIRE AND TRAXCESS DOCKING WIRE
Manufacturer: MICROVENTION, INC.
Device Classification Name: wire, guide, catheter
Regulation Number: 870.1330
Classification Product Code: DQX
Date Received: 10/30/2009
Decision Date: 12/17/2009
Regulation Medical Specialty: Cardiovascular
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