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CORDIS M3 PTA DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003920
510(k) Type
Abbreviated
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
178 days
Submission Type
Summary

CORDIS M3 PTA DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003920
510(k) Type
Abbreviated
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
178 days
Submission Type
Summary