FDA 510(k) Application Details - K173290

Device Classification Name	Coil, Magnetic Resonance, Specialty   More FDA Info for this Device
510(K) Number	K173290
Device Name	Coil, Magnetic Resonance, Specialty
Applicant	MR Instruments, Inc 5610 Rowland Road, Suite 145 Minnetonka, MN 55343 US Other 510(k) Applications for this Company
Contact	Leon Ricord Other 510(k) Applications for this Contact
Regulation Number	892.1000   More FDA Info for this Regulation Number
Classification Product Code	MOS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/16/2017
Decision Date	11/28/2017
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	Y
Expedited Review