FDA 510(k) Application Details - K242925

Device Classification Name	More FDA Info for this Device
510(K) Number	K242925
Device Name	MR Contour DL
Applicant	GE HealthCare 500 W. Monroe Street Chicago, IL 60661 US Other 510(k) Applications for this Company
Contact	Allena Holzworth Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QKB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/24/2024
Decision Date	04/01/2025
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