FDA 510(k) Application Details - K980235

Device Classification Name	System, X-Ray, Mammographic   More FDA Info for this Device
510(K) Number	K980235
Device Name	System, X-Ray, Mammographic
Applicant	KCI NEW TECHNOLOGIES, INC. P.O. BOX 659508 SAN ANTONIO, TX 78265 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	01/22/1998
Decision Date	04/09/1998
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