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MODIFICATION TO FIDIS VASCULITIS, MODEL MX007

Page Type
Cleared 510(K)
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)
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