FDA 510(k), SmartCardia 7L Platform, Steurer Consulting Group LLC

FDA 510(k), SmartCardia 7L Platform, Steurer Consulting Group LLC

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510(K) Number: K231276
Device Name: SmartCardia 7L Platform
Manufacturer: Steurer Consulting Group LLC
Device Classification Name: Detector And Alarm, Arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 05/02/2023
Decision Date: 08/30/2023
Regulation Medical Specialty: Cardiovascular
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