FDA 510(k) Application Details - K240177

Device Classification Name	Detector And Alarm, Arrhythmia   More FDA Info for this Device
510(K) Number	K240177
Device Name	Detector And Alarm, Arrhythmia
Applicant	iRhythm Technologies, Inc. 699 8th Street Suite 600 San Francisco, CA 94103 US Other 510(k) Applications for this Company
Contact	Soyini Hamit 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	01/23/2024
Decision Date	10/30/2024
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