FDA 510(k), K133725, TRAXCESS 14 GUIDEWIRE
FDA 510(k), K133725, TRAXCESS 14 GUIDEWIRE
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510(K) Number: K133725
Device Name: TRAXCESS 14 GUIDEWIRE
Manufacturer: MICROVENTION, INC.
Device Classification Name: guide, wire, catheter, neurovasculature
Regulation Number: 870.1330
Classification Product Code: MOF
Date Received: 12/06/2013
Decision Date: 07/31/2014
Regulation Medical Specialty: Cardiovascular
Device Name: TRAXCESS 14 GUIDEWIRE
Manufacturer: MICROVENTION, INC.
Device Classification Name: guide, wire, catheter, neurovasculature
Regulation Number: 870.1330
Classification Product Code: MOF
Date Received: 12/06/2013
Decision Date: 07/31/2014
Regulation Medical Specialty: Cardiovascular
- 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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