FDA 510(k) Application Details - K210760

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K210760
Device Name	System, X-Ray, Tomography, Computed
Applicant	Philips Medical Systems Nederland, B.V. Veenpluis 4-6 Best Noord-Brabant 5684 PC NL Other 510(k) Applications for this Company
Contact	Michael Chilbert Other 510(k) Applications for this Contact
Regulation Number	892.1750   More FDA Info for this Regulation Number
Classification Product Code	JAK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/15/2021
Decision Date	01/14/2022
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