FDA 510(k), K901337, HILAL EMBOLIZATION MICROCOIL(TM)

FDA 510(k), K901337, HILAL EMBOLIZATION MICROCOIL(TM)

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510(K) Number: K901337
Device Name: HILAL EMBOLIZATION MICROCOIL(TM)
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 03/22/1990
Decision Date: 11/13/1990
Regulation Medical Specialty: Neurology
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