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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