FDA 510(k) Application Details - K051932

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K051932
Device Name	Accelerator, Linear, Medical
Applicant	ELEKTA, INC 4775 PEACHTREE IND. BLVD BUILDING 300, SUITE 300 NORCROSS, GA 30092 US Other 510(k) Applications for this Company
Contact	PETER STEGAGNO 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	07/13/2005
Decision Date	08/12/2005
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