FDA 510(k) Application Details - K131737

Device Classification Name	System, Nuclear Magnetic Resonance Imaging   More FDA Info for this Device
510(K) Number	K131737
Device Name	System, Nuclear Magnetic Resonance Imaging
Applicant	LIAONING KAMPO MEDICAL SYSTEM CO., LTD. NO. 9, YAODU STREET, BENXI ECONOMIC DEVELOPMENT AREA BENXI, LIAONING 117004 CN Other 510(k) Applications for this Company
Contact	SHAO KAI Other 510(k) Applications for this Contact
Regulation Number	892.1000   More FDA Info for this Regulation Number
Classification Product Code	LNH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/13/2013
Decision Date	10/23/2014
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