FDA 510(k) Application Details - K240680

Device Classification Name	More FDA Info for this Device
510(K) Number	K240680
Device Name	CDM Insights
Applicant	Oxford Brain Diagnostics Ltd Oxford Centre for Innovation, New Road Oxford OX1 1BY GB Other 510(k) Applications for this Company
Contact	Terry Pollard Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/11/2024
Decision Date	12/06/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review