FDA 510(k) Application Details - K100692

Device Classification Name	System, X-Ray, Mammographic   More FDA Info for this Device
510(K) Number	K100692
Device Name	System, X-Ray, Mammographic
Applicant	HOLOGIC, INC. 36 APPLE RIDGE ROAD DANBURY, CT 06810 US Other 510(k) Applications for this Company
Contact	GAIL YAEKER-DAUNIS 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	03/10/2010
Decision Date	04/06/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review