FDA 510(k), K171845, EMBA Hourglass Peripheral Embolization Device
FDA 510(k), K171845, EMBA Hourglass Peripheral Embolization Device
Device Name: EMBA Hourglass Peripheral Embolization Device
Manufacturer:
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 06/20/2017
Decision Date: 08/18/2017
Regulation Medical Specialty: Cardiovascular
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