FDA 510(k) Application Details - K161920

Device Classification Name	System, X-Ray, Mammographic   More FDA Info for this Device
510(K) Number	K161920
Device Name	System, X-Ray, Mammographic
Applicant	PRECISION DYNAMICS CORPORATION 27770 ENTERTAINMENT DRIVE, STE 200 VALENCIA, CA 91355 US Other 510(k) Applications for this Company
Contact	SWARNA MUKUND Other 510(k) Applications for this Contact
Regulation Number	892.1710   More FDA Info for this Regulation Number
Classification Product Code	IZH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/13/2016
Decision Date	07/15/2016
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	Y
Expedited Review