FDA 510(k), K093647, TRAXCESS DOCKING WIRE

FDA 510(k), K093647, TRAXCESS DOCKING WIRE

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510(K) Number: K093647
Device Name: TRAXCESS DOCKING WIRE
Manufacturer: MICROVENTION, INC.
Device Classification Name: wire, guide, catheter
Regulation Number: 870.1330
Classification Product Code: DQX
Date Received: 11/25/2009
Decision Date: 02/24/2010
Regulation Medical Specialty: Cardiovascular

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