FDA 510(k) Application Details - K013279

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K013279
Device Name	Accelerator, Linear, Medical
Applicant	THOMSON & NIELSEN ELECTRONICS, LTD. 25-B NORTHSIDE RD. OTTAWA, ONTARIO K2H 8S1 CA Other 510(k) Applications for this Company
Contact	NORMA THOMSON Other 510(k) Applications for this Contact
Regulation Number	892.5050   More FDA Info for this Regulation Number
Classification Product Code	IYE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/02/2001
Decision Date	10/18/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review