FDA 510(k) Application Details - K042095

Device Classification Name	System, X-Ray, Mammographic   More FDA Info for this Device
510(K) Number	K042095
Device Name	System, X-Ray, Mammographic
Applicant	FISCHER IMAGING CORP. 12300 NORTH GRANT ST. DENVER, CO 80241-3120 US Other 510(k) Applications for this Company
Contact	ROBERT G SCHUEPPERT 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	08/03/2004
Decision Date	10/29/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review