Neusoft Digital Medical Systems Co., Ltd. is one of 2194 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
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
Neusoft Digital Medical Systems Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Shenyang, Liaoning, CN.
Historical record: 4 cleared submissions from 2002 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Neusoft Digital Medical Systems Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neusoft Digital Medical Systems Co., Ltd.
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