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AGILTRAC .035 PERIPHERAL DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023320
510(k) Type
Traditional
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2002
Days to Decision
67 days
Submission Type
Summary

AGILTRAC .035 PERIPHERAL DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023320
510(k) Type
Traditional
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2002
Days to Decision
67 days
Submission Type
Summary