FDA 510(k) Application Details - K092899

Device Classification Name	System, Nuclear Magnetic Resonance Imaging   More FDA Info for this Device
510(K) Number	K092899
Device Name	System, Nuclear Magnetic Resonance Imaging
Applicant	NINGBO XINGAOYI MAGNETISM CO., LTD. EAST TANJIALING RD. YUYAO, ZHEJIANG 315400 CN Other 510(k) Applications for this Company
Contact	JIANG MOWEN 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	09/21/2009
Decision Date	11/10/2009
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	Y
Expedited Review