FDA 510(k) Application Details - K142294

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K142294
Device Name	Accelerator, Linear, Medical
Applicant	CORTEX MANUFACTURING, INC. 421 South Davies Rd. Lake Stevens, WA 98258 US Other 510(k) Applications for this Company
Contact	Andrew Jones 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	08/18/2014
Decision Date	03/26/2015
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