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POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112797
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2012
Days to Decision
221 days
Submission Type
Summary

POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112797
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2012
Days to Decision
221 days
Submission Type
Summary