FDA 510(k), K081942, NEUROCATH AG

FDA 510(k), K081942, NEUROCATH AG

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510(K) Number: K081942
Device Name: NEUROCATH AG
Manufacturer:
Device Classification Name: Shunt, Central Nervous System And Components
Regulation Number: 882.5550
Classification Product Code: JXG
Date Received: 07/08/2008
Decision Date: 08/12/2008
Regulation Medical Specialty: Neurology
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