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FDA 510(k), K123384, AZUR CX DETACHABLE 18
FDA 510(k), K123384, AZUR CX DETACHABLE 18
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510(K) Number: K123384
Device Name: AZUR CX DETACHABLE 18
Manufacturer: MICROVENTION, INC.
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 11/02/2012
Decision Date: 11/28/2012
Regulation Medical Specialty: Cardiovascular
Device Name: AZUR CX DETACHABLE 18
Manufacturer: MICROVENTION, INC.
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 11/02/2012
Decision Date: 11/28/2012
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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