FDA 510(k), K983483, VASCULAR OCCLUSION SYSTEM
FDA 510(k), K983483, VASCULAR OCCLUSION SYSTEM
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510(K) Number: K983483
Device Name: VASCULAR OCCLUSION SYSTEM
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 10/05/1998
Decision Date: 03/24/1999
Regulation Medical Specialty: Neurology
Device Name: VASCULAR OCCLUSION SYSTEM
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 10/05/1998
Decision Date: 03/24/1999
Regulation Medical Specialty: Neurology