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SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter

Page Type
Cleared 510(K)
510(k) Number
K201377
510(k) Type
Traditional
Applicant
Cordis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2020
Days to Decision
136 days
Submission Type
Summary

SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter

Page Type
Cleared 510(K)
510(k) Number
K201377
510(k) Type
Traditional
Applicant
Cordis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2020
Days to Decision
136 days
Submission Type
Summary