FDA 510(k) Application Details - K141230

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K141230
Device Name	Accelerator, Linear, Medical
Applicant	MOBIUS MEDICAL SYSTEMS, LP 5012 TAMARISK ST. BELLAIRE, TX 77401 US Other 510(k) Applications for this Company
Contact	STAN ESHELMAN 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	05/13/2014
Decision Date	08/27/2014
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