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ViaValve Safety I.V. Catheter

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