FDA 510(k) Application Details - K203020

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K203020
Device Name	System, X-Ray, Tomography, Computed
Applicant	Philips Medical Systems Nederland B.V. Veenpluis 4-6 Best 5684 PC NL Other 510(k) Applications for this Company
Contact	Yaara Oltchik 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	10/02/2020
Decision Date	02/26/2021
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