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CT-C3000DUAL AND CT-C2800DUAL FAMILY OF DUAL-SLICE CT SCANNER SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041542
510(k) Type
Traditional
Applicant
NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/17/2004
Days to Decision
9 days
Submission Type
Summary

CT-C3000DUAL AND CT-C2800DUAL FAMILY OF DUAL-SLICE CT SCANNER SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041542
510(k) Type
Traditional
Applicant
NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/17/2004
Days to Decision
9 days
Submission Type
Summary