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CARDEON AEGIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K013593
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2002
Days to Decision
237 days
Submission Type
Summary

CARDEON AEGIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K013593
510(k) Type
Traditional
Applicant
CARDEON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2002
Days to Decision
237 days
Submission Type
Summary