FDA 510(k) Application Details - K173145

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K173145
Device Name	System, Image Processing, Radiological
Applicant	CereMetrix Corp 991 Southpark Drive , Suite 200 Littleton, CO 80120 US Other 510(k) Applications for this Company
Contact	John A Kelley Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	LLZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2017
Decision Date	02/28/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review