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CORDIS M3 PTA DILATATION CATHETER

Page Type
Cleared 510(K)
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)
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