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FDA 510(k) K092780, INF 4160 PLUS, MODEL D-FJ31F, by Fuji Dynamics Limited

FDA 510(k) K092780, INF 4160 PLUS, MODEL D-FJ31F, by Fuji Dynamics Limited

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510(K) Number: K092780
Device Name: INF 4160 PLUS, MODEL D-FJ31F
Manufacturer: Fuji Dynamics Limited
Device Classification Name: interferential current therapy
Regulation Number: 882.5890
Classification Product Code: LIH
Date Received: 09/10/2009
Decision Date: 01/07/2010
Regulation Medical Specialty: Neurology
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