FDA 510(k) Application Details - K161563

Device Classification Name	More FDA Info for this Device
510(K) Number	K161563
Device Name	Allura Xper FD series and Allura Xper OR Table series
Applicant	Philips Medical Systems Nederland BV VEENPLUIS 4-6 BEST 5684PC NL Other 510(k) Applications for this Company
Contact	Jeanette Becker Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/06/2016
Decision Date	07/29/2016
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