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FDA 510(k) Applications Submitted by NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020913
03/21/2002
CT-C3000 SPIRAL CT SCANNER SYSTEM
NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD.
K030918
03/24/2003
SUPEROPEN 0.35T, MODEL NSM-P035
NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD.
K041542
06/08/2004
CT-C3000DUAL AND CT-C2800DUAL FAMILY OF DUAL-SLICE CT SCANNER SYSTEMS
NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD.
K033315
10/15/2003
SUPEROPEN 0.23T, MODEL NAM-P023A
NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD.
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