FDA 510(k), K912938, RHYTHM

FDA 510(k), K912938, RHYTHM

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510(K) Number: K912938
Device Name: RHYTHM
Manufacturer: STELLATE SYSTEMS
Device Classification Name: analyzer, spectrum, electroencephalogram signal
Regulation Number: 882.1420
Classification Product Code: GWS
Date Received: 07/05/1991
Decision Date: 07/30/1991
Regulation Medical Specialty: Neurology
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