FDA 510(k) Application Details - K210692

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K210692
Device Name	System, X-Ray, Stationary
Applicant	Philips Medical Systems DMC GmbH Roentgenstrasse 24-26 Hamburg 22335 DE Other 510(k) Applications for this Company
Contact	Supriya Dalvi Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/08/2021
Decision Date	04/02/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review