FDA 510(k) Application Details - K973400

Device Classification Name	System, X-Ray, Mammographic   More FDA Info for this Device
510(K) Number	K973400
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	SAMMUELLA D ENRICH 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	09/09/1997
Decision Date	11/10/1997
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