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FDA 510(k), K120917, HEADWAY DUO MICROCATHETER
FDA 510(k), K120917, HEADWAY DUO MICROCATHETER
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510(K) Number: K120917
Device Name: HEADWAY DUO MICROCATHETER
Manufacturer: MICROVENTION, INC.
Device Classification Name: catheter, intravascular, diagnostic
Regulation Number: 870.1200
Classification Product Code: DQO
Date Received: 03/27/2012
Decision Date: 08/02/2012
Regulation Medical Specialty: Cardiovascular
Device Name: HEADWAY DUO MICROCATHETER
Manufacturer: MICROVENTION, INC.
Device Classification Name: catheter, intravascular, diagnostic
Regulation Number: 870.1200
Classification Product Code: DQO
Date Received: 03/27/2012
Decision Date: 08/02/2012
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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