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FDA 510(k) K152139, Vital Connect Platform, HealthPatch MD, VitalPatch, by Vitalconnect, Inc.

FDA 510(k) K152139, Vital Connect Platform, HealthPatch MD, VitalPatch, by Vitalconnect, Inc.

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510(K) Number: K152139
Device Name: Vital Connect Platform, HealthPatch MD, VitalPatch
Manufacturer: Vitalconnect, Inc.
Device Classification Name: Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation Number: DRG
Classification Product Code: KXA
Date Received: 08/03/2015
Decision Date: 12/06/2015
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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