FDA 510(k), K072343, NEUROVISION JJB SYSTEM

FDA 510(k), K072343, NEUROVISION JJB SYSTEM

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510(K) Number: K072343
Device Name: NEUROVISION JJB SYSTEM
Manufacturer:
Device Classification Name: Stimulator, Electrical, Evoked Response
Regulation Number: 882.1870
Classification Product Code: GWF
Date Received: 08/21/2007
Decision Date: 10/29/2007
Regulation Medical Specialty: Neurology
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