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CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K063563
510(k) Type
Traditional
Applicant
CORDIS EUROPA, N.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2007
Days to Decision
99 days
Submission Type
Summary

CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K063563
510(k) Type
Traditional
Applicant
CORDIS EUROPA, N.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2007
Days to Decision
99 days
Submission Type
Summary