FDA 510(k) Application Details - K173821

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K173821
Device Name	System, X-Ray, Tomography, Computed
Applicant	Thirona Corporation Toernooiveld 300 Nijmegen 6525 EC NL Other 510(k) Applications for this Company
Contact	Eva van Rikxoort 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	12/18/2017
Decision Date	06/05/2018
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