FDA 510(k), K170568, CardioLogs ECG Analysis Platform

FDA 510(k), K170568, CardioLogs ECG Analysis Platform

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510(K) Number: K170568
Device Name: CardioLogs ECG Analysis Platform
Manufacturer: Cardiologs Technologies
Device Classification Name: electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 02/27/2017
Decision Date: 06/26/2017
Regulation Medical Specialty: Cardiovascular

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