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Ultraverse 014 and 018 PTA Balloon Dilatation Catheters

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192318
510(k) Type
Traditional
Applicant
Bard Peripheral Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2019
Days to Decision
38 days
Submission Type
Summary

Ultraverse 014 and 018 PTA Balloon Dilatation Catheters

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192318
510(k) Type
Traditional
Applicant
Bard Peripheral Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2019
Days to Decision
38 days
Submission Type
Summary