FDA 510(k) Application Details - K163282

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K163282
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	Masterlink LLC 24654 N. Lake Pleasant Parkway Suite 103-501 Peoria, AZ 85383 US Other 510(k) Applications for this Company
Contact	Tom Birney 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	11/21/2016
Decision Date	02/28/2017
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