FDA 510(k) Application Details - K232644

Device Classification Name	System, Nuclear Magnetic Resonance Imaging   More FDA Info for this Device
510(K) Number	K232644
Device Name	System, Nuclear Magnetic Resonance Imaging
Applicant	Neuro42, Inc. 2 Bryant Street, Suite 240 San Francisco, CA 94105 US Other 510(k) Applications for this Company
Contact	Abhita Batra 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	08/30/2023
Decision Date	02/08/2024
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