FDA 510(k), K050036, FES CYCLE ERGOMETER, MODEL RT300-S

FDA 510(k), K050036, FES CYCLE ERGOMETER, MODEL RT300-S

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510(K) Number: K050036
Device Name: FES CYCLE ERGOMETER, MODEL RT300-S
Manufacturer:
Device Classification Name: Stimulator, Neuromuscular, External Functional
Regulation Number: 882.5810
Classification Product Code: GZI
Date Received: 01/07/2005
Decision Date: 06/27/2005
Regulation Medical Specialty: Neurology
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