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SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter

Page Type
Cleared 510(K)
510(k) Number
K210626
510(k) Type
Traditional
Applicant
Cordis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2021
Days to Decision
52 days
Submission Type
Summary

SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter

Page Type
Cleared 510(K)
510(k) Number
K210626
510(k) Type
Traditional
Applicant
Cordis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2021
Days to Decision
52 days
Submission Type
Summary