FDA 510(k) Application Details - K150725

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K150725
Device Name	System, X-Ray, Stationary
Applicant	VISARIS d.o.o. Belgrade Batajnicki drum 10 deo 1b Zemun 11080 RS Other 510(k) Applications for this Company
Contact	Milan Ratkovic Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/20/2015
Decision Date	06/08/2015
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