FDA 510(k) Application Details - K193215

Device Classification Name	System, Nuclear Magnetic Resonance Imaging   More FDA Info for this Device
510(K) Number	K193215
Device Name	System, Nuclear Magnetic Resonance Imaging
Applicant	Philips Medical Systems Nederland BV Veenpluis 4-6 Best 5684PC NL Other 510(k) Applications for this Company
Contact	Jan Van de Kerkhof 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	11/21/2019
Decision Date	04/10/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review