FDA 510(k) Application Details - K090366

Device Classification Name	Source, Brachytherapy, Radionuclide   More FDA Info for this Device
510(K) Number	K090366
Device Name	Source, Brachytherapy, Radionuclide
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	892.5730   More FDA Info for this Regulation Number
Classification Product Code	KXK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/13/2009
Decision Date	04/22/2009
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