FDA 510(k) Application Details - K220786

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K220786
Device Name	Computer, Diagnostic, Programmable
Applicant	Rhythm Al, Ltd Office G2, Whitney Business and Innovation, Windrush House, Buford Rd Witney OX 29 7DX GB Other 510(k) Applications for this Company
Contact	Linda D'Abate Other 510(k) Applications for this Contact
Regulation Number	870.1425   More FDA Info for this Regulation Number
Classification Product Code	DQK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/17/2022
Decision Date	12/01/2022
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