FDA 510(k) Application Details - K142995

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K142995
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	SOPRO - ACTEON GROUP LaCiotat 13705 FR Other 510(k) Applications for this Company
Contact	PHILIPPE BOYER Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	MUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/16/2014
Decision Date	08/17/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review