FDA 510(k) Application Details - K250901

Device Classification Name	System, Nuclear Magnetic Resonance Imaging   More FDA Info for this Device
510(K) Number	K250901
Device Name	System, Nuclear Magnetic Resonance Imaging
Applicant	Canon Medical Systems Corporation 1385 Shimoishigami Otawara-shi 3248550 JP Other 510(k) Applications for this Company
Contact	Orlando Tadeo Other 510(k) Applications for this Contact
Regulation Number	892.1000   More FDA Info for this Regulation Number
Classification Product Code	LNH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/26/2025
Decision Date	07/22/2025
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