FDA 510(k) Application Details - K110849

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K110849
Device Name	System, X-Ray, Stationary
Applicant	CMT MEDICAL TECHNOLOGIES, LTD. INDUSTRIAL PARK P.O.B. 111 YOQNEAM ILIT 20692 IL Other 510(k) Applications for this Company
Contact	SHLOMI DINES Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/28/2011
Decision Date	04/26/2011
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