FDA 510(k) Application Details - K973915

Device Classification Name	System, X-Ray, Mammographic   More FDA Info for this Device
510(K) Number	K973915
Device Name	System, X-Ray, Mammographic
Applicant	KCI NEW TECHNOLOGIES, INC. 3440 EAST HOUSTON SAN ANTONIO, TX 78219 US Other 510(k) Applications for this Company
Contact	JUDITH A HARBOUR 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	10/14/1997
Decision Date	11/10/1997
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