FDA 510(k) Application Details - K133972

Device Classification Name	Full Field Digital,System,X-Ray,Mammographic   More FDA Info for this Device
510(K) Number	K133972
Device Name	Full Field Digital,System,X-Ray,Mammographic
Applicant	FUJIFILM MEDICAL SYSTEMS, USA INC. 419 WEST AVE. STANFORD, CT 06902 US Other 510(k) Applications for this Company
Contact	PETER ALTMAN Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MUE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/26/2013
Decision Date	03/25/2014
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