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SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K133843
510(k) Type
Traditional
Applicant
CORDIS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2014
Days to Decision
191 days
Submission Type
Summary

SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K133843
510(k) Type
Traditional
Applicant
CORDIS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2014
Days to Decision
191 days
Submission Type
Summary