FDA 510(k) Application Details - K223094

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K223094
Device Name	Computer, Diagnostic, Programmable
Applicant	Abbott Medical One St. Jude Medical Device St. Paul, MN 55117 US Other 510(k) Applications for this Company
Contact	Alyssa Timmers 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	09/30/2022
Decision Date	12/27/2022
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