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ViaValve Safety I.V. Catheter

Page Type
Cleared 510(K)
510(k) Number
K160235
510(k) Type
Traditional
Applicant
SMITHS MEDICAL ASD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2016
Days to Decision
150 days
Submission Type
Summary

ViaValve Safety I.V. Catheter

Page Type
Cleared 510(K)
510(k) Number
K160235
510(k) Type
Traditional
Applicant
SMITHS MEDICAL ASD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2016
Days to Decision
150 days
Submission Type
Summary