Neusoft Digital Medical Systems Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CT-C3000DUAL AND CT-C2800DUAL FAMILY OF DUAL-SLICE CT SCANNER SYSTEMS, SUPEROPEN 0.23T, MODEL NAM-P023A, SUPEROPEN 0.35T, MODEL NSM-P035
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Neusoft Digital Medical Systems Co., Ltd. Radiology ✕
4 devices
Cleared
Jun 17, 2004
CT-C3000DUAL AND CT-C2800DUAL FAMILY OF DUAL-SLICE CT SCANNER SYSTEMS
Radiology
9d
Cleared
Oct 29, 2003
SUPEROPEN 0.23T, MODEL NAM-P023A
Radiology
14d
Cleared
Apr 01, 2003
SUPEROPEN 0.35T, MODEL NSM-P035
Radiology
8d
Cleared
Apr 03, 2002
CT-C3000 SPIRAL CT SCANNER SYSTEM
Radiology
13d