FDA 510(k) Application Details - K013660

Device Classification Name	Source, Brachytherapy, Radionuclide   More FDA Info for this Device
510(K) Number	K013660
Device Name	Source, Brachytherapy, Radionuclide
Applicant	RADIOMED CORPORATION ONE INDUSTRIAL WAY TYNGSBORO, MA 01879-1400 US Other 510(k) Applications for this Company
Contact	GORDON ROBERTS 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	11/06/2001
Decision Date	12/05/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review