FDA 510(k), K021100, 300 PV COMPLETE ELECTROTHERAPY SYSTEM

FDA 510(k), K021100, 300 PV COMPLETE ELECTROTHERAPY SYSTEM

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510(K) Number: K021100
Device Name: 300 PV COMPLETE ELECTROTHERAPY SYSTEM
Manufacturer: EMPI
Device Classification Name: stimulator, muscle, powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 04/04/2002
Decision Date: 06/18/2002
Regulation Medical Specialty: Physical Medicine

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