FDA 510(k) Application Details - K060532

Device Classification Name	System, Applicator, Radionuclide, Remote-Controlled   More FDA Info for this Device
510(K) Number	K060532
Device Name	System, Applicator, Radionuclide, Remote-Controlled
Applicant	STANDARD IMAGING, INC. 7601 MURPHY DR. MIDDLETON, WI 53562-2766 US Other 510(k) Applications for this Company
Contact	RAYMOND RIDDLE Other 510(k) Applications for this Contact
Regulation Number	892.5700   More FDA Info for this Regulation Number
Classification Product Code	JAQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/28/2006
Decision Date	04/11/2006
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