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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