FDA 510(k), K132317, MICROPLEX COIL SYSTEM (MCS), VFC

FDA 510(k), K132317, MICROPLEX COIL SYSTEM (MCS), VFC

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510(K) Number: K132317
Device Name: MICROPLEX COIL SYSTEM (MCS), VFC
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 07/25/2013
Decision Date: 09/20/2013
Regulation Medical Specialty: Neurology
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