FDA 510(k) Applications Submitted by TIAN YANFANG

FDA 510(k) Number Submission Date Device Name Applicant
K090173 01/23/2009 NEUVIZ 16 MULTI-SLICE CT SCANNER SYSTEM NEUSOFT MEDICAL SYSTEMS CO., LTD.
K080540 02/27/2008 NEUSOFT SPIRAL CT SCANNER SYSTEM, MODEL NEUVIZ VERSION 2.0 NEUSOFT MEDICAL SYSTEMS CO., LTD.
K090552 03/02/2009 UROCARE NEUSOFT MEDICAL SYSTEMS CO., LTD.
K061132 04/24/2006 MODIFICATION TO SUPEROPEN 0.35T, MODEL NSM-P035 NEUSOFT MEDICAL SYSTEMS CO., LTD.
K071308 05/09/2007 MODIFICATION TO NEUVIZ DUAL MULTI-SLICE CT SCANNER SYSTEM NEUSOFT MEDICAL SYSTEMS CO., LTD.
K062451 08/22/2006 NEUVIZ DUAL MULTI-SLICE CT SCANNER SYSTEM NEUSOFT MEDICAL SYSTEMS CO., LTD.
K082485 08/28/2008 MODIFICATION TO SUPEROPEN 0.23T MRI SYSTEM, MODEL NAM-P023A NEUSOFT MEDICAL SYSTEMS CO., LTD.
K062860 09/25/2006 MODIFICATION TO SUPEROPEN 0.23T, MODEL NAM-P023A NEUSOFT MEDICAL SYSTEMS CO., LTD.
K083877 12/29/2008 FLYING DIAGNOSTIC ULTRASOUND SYSTEM NEUSOFT MEDICAL SYSTEMS CO., LTD.


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