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VIATRONIX V3D VASCULAR, REVISION 1.0

Page Type
Cleared 510(K)
510(k) Number
K033361
510(k) Type
Traditional
Applicant
VIATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
15 days
Submission Type
Summary

VIATRONIX V3D VASCULAR, REVISION 1.0

Page Type
Cleared 510(K)
510(k) Number
K033361
510(k) Type
Traditional
Applicant
VIATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
15 days
Submission Type
Summary