FDA 510(k), K183078, VitalConnect Platform, VitalPatch Biosensor

FDA 510(k), K183078, VitalConnect Platform, VitalPatch Biosensor

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510(K) Number: K183078
Device Name: VitalConnect Platform, VitalPatch Biosensor
Manufacturer: VitalConnect, Inc.
Device Classification Name: Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation Number: 870.2910
Classification Product Code: DRG
Date Received: 11/05/2018
Decision Date: 03/07/2019
Regulation Medical Specialty: Cardiovascular

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