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CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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