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FDA 510(k), K113658, AMPLATZER VASCULAR PLUG 4
FDA 510(k), K113658, AMPLATZER VASCULAR PLUG 4
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510(K) Number: K113658
Device Name: AMPLATZER VASCULAR PLUG 4
Manufacturer: AGA MEDICAL CORP.
Device Classification Name: device, vascular, for promoting embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 12/12/2011
Decision Date: 06/12/2012
Regulation Medical Specialty: Cardiovascular
Device Name: AMPLATZER VASCULAR PLUG 4
Manufacturer: AGA MEDICAL CORP.
Device Classification Name: device, vascular, for promoting embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 12/12/2011
Decision Date: 06/12/2012
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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