FDA 510(k) Application Details - K052947

Device Classification Name	System, Applicator, Radionuclide, Remote-Controlled   More FDA Info for this Device
510(K) Number	K052947
Device Name	System, Applicator, Radionuclide, Remote-Controlled
Applicant	SOURCE PRODUCTION & EQUIPMENT CO., INC. 113 TEAL STREET ST. ROSE, LA 70087 US Other 510(k) Applications for this Company
Contact	JOHN J MUNRO 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	10/20/2005
Decision Date	04/19/2006
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