• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K113658, AMPLATZER VASCULAR PLUG 4, by Aga Medical Corp.

FDA 510(k) K113658, AMPLATZER VASCULAR PLUG 4, by Aga Medical Corp.

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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

Total pages: 7366
Fully redacted pages: 6923
Content pages: 443
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