Last synced on 14 November 2025 at 11:06 pm

VIATRONIX V3D EXPLORER, REVISION 1.2

Page Type
Cleared 510(K)
510(k) Number
K032483
510(k) Type
Traditional
Applicant
VIATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
10 days
Submission Type
Summary

VIATRONIX V3D EXPLORER, REVISION 1.2

Page Type
Cleared 510(K)
510(k) Number
K032483
510(k) Type
Traditional
Applicant
VIATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
10 days
Submission Type
Summary