FDA 510(k) Application Details - K231276

Device Classification Name	Detector And Alarm, Arrhythmia   More FDA Info for this Device
510(K) Number	K231276
Device Name	Detector And Alarm, Arrhythmia
Applicant	SmartCardia SA EPFL Innovation Park Building C Lausanne 1015 CH Other 510(k) Applications for this Company
Contact	Srinivasan Murali Other 510(k) Applications for this Contact
Regulation Number	870.1025   More FDA Info for this Regulation Number
Classification Product Code	DSI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/02/2023
Decision Date	08/30/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review