FDA 510(k) Application Details - K042671

Device Classification Name	System, X-Ray, Mammographic   More FDA Info for this Device
510(K) Number	K042671
Device Name	System, X-Ray, Mammographic
Applicant	PLANMED OY 100 NORTH GRAY AVE. SUITE A ROSELLE, IL 60172 US Other 510(k) Applications for this Company
Contact	BOB PIENKOWSKI 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	09/29/2004
Decision Date	11/19/2004
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