Last synced on 25 January 2026 at 3:41 am

SABER .014 PTA Dilatation Catheter; SABERX .014 PTA Dilatation Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221832
510(k) Type
Traditional
Applicant
Cordis US Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2022
Days to Decision
60 days
Submission Type
Summary

SABER .014 PTA Dilatation Catheter; SABERX .014 PTA Dilatation Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221832
510(k) Type
Traditional
Applicant
Cordis US Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2022
Days to Decision
60 days
Submission Type
Summary