FDA 510(k) Application Details - K182973

Device Classification Name	Solid State X-Ray Imager (Flat Panel/Digital Imager)   More FDA Info for this Device
510(K) Number	K182973
Device Name	Solid State X-Ray Imager (Flat Panel/Digital Imager)
Applicant	Philips Medical Systems DMC GmbH Roentgenstrasse 24 Hamburg 22335 DE Other 510(k) Applications for this Company
Contact	Ming Xiao Other 510(k) Applications for this Contact
Regulation Number	892.1650   More FDA Info for this Regulation Number
Classification Product Code	MQB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/26/2018
Decision Date	01/11/2019
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