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MODIFICATION TO FIDIS VASCULITIS, MODEL MX007

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070458
510(k) Type
Traditional
Applicant
Biomedical Diagnostics (Bmd) SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/21/2007
Days to Decision
308 days
Submission Type
Summary

MODIFICATION TO FIDIS VASCULITIS, MODEL MX007

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070458
510(k) Type
Traditional
Applicant
Biomedical Diagnostics (Bmd) SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/21/2007
Days to Decision
308 days
Submission Type
Summary