FDA 510(k) Application Details - K183034

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K183034
Device Name	Accelerator, Linear, Medical
Applicant	Elekta, Inc 100 Mathilda Place 5th Floor Sunnyvale, CA 94086 US Other 510(k) Applications for this Company
Contact	Faiza Ahmed 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	11/01/2018
Decision Date	12/04/2018
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