FDA 510(k) Application Details - K232974

Device Classification Name	Electrocardiograph   More FDA Info for this Device
510(K) Number	K232974
Device Name	Electrocardiograph
Applicant	EKGenius LLC 347 Clinton St Hempstead, NY 11550 US Other 510(k) Applications for this Company
Contact	Shachar Barel Other 510(k) Applications for this Contact
Regulation Number	870.2340   More FDA Info for this Regulation Number
Classification Product Code	DPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/21/2023
Decision Date	11/17/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review