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FDA 510(k) K141813, RHYTHMSTAR SYSTEM, by RhythMedix, LLC

FDA 510(k) K141813, RHYTHMSTAR SYSTEM, by RhythMedix, LLC

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510(K) Number: K141813
Device Name: RHYTHMSTAR SYSTEM
Manufacturer: RhythMedix, LLC
Device Classification Name: transmitters and receivers, electrocardiograph, telephone
Regulation Number: 870.2920
Classification Product Code: DXH
Date Received: 07/07/2014
Decision Date: 08/05/2014
Regulation Medical Specialty: Cardiovascular
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