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VIATRONIX V3D VASCULAR, REVISION 1.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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