FDA 510(k) Application Details - K062823

Device Classification Name	System, Applicator, Radionuclide, Remote-Controlled   More FDA Info for this Device
510(K) Number	K062823
Device Name	System, Applicator, Radionuclide, Remote-Controlled
Applicant	ALPHA-OMEGA SERVICES, INC. 9156 ROSE ST BELLFLOWER, CA 90706 US Other 510(k) Applications for this Company
Contact	BOB A ROBNETT 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	09/20/2006
Decision Date	05/29/2007
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