FDA 510(k) Application Details - K243842

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K243842
Device Name	Computer, Diagnostic, Programmable
Applicant	Centerline Biomedical, Inc. 4535 Renaissance Pkwy Cleveland, OH 44128 US Other 510(k) Applications for this Company
Contact	Amanda Shade 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	12/13/2024
Decision Date	03/06/2025
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