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POWERFLEX(TM) 5F PTA BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K946052
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1995
Days to Decision
81 days
Submission Type
Summary

POWERFLEX(TM) 5F PTA BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K946052
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1995
Days to Decision
81 days
Submission Type
Summary