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VIATRONIX V3D COLON, REVISION 1.3

Page Type
Cleared 510(K)
510(k) Number
K040126
510(k) Type
Traditional
Applicant
VIATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2004
Days to Decision
90 days
Submission Type
Summary

VIATRONIX V3D COLON, REVISION 1.3

Page Type
Cleared 510(K)
510(k) Number
K040126
510(k) Type
Traditional
Applicant
VIATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2004
Days to Decision
90 days
Submission Type
Summary