FDA 510(k), K113658, AMPLATZER VASCULAR PLUG 4

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