FDA 510(k) Application Details - K152162

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K152162
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	CEFLA S.C. VIA SELICE PROVINCIALE 23/A IMOLA 40026 IT Other 510(k) Applications for this Company
Contact	Silvia Sansavini 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	08/03/2015
Decision Date	12/24/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review