Last synced on 18 April 2025 at 11:05 pm

AGILTRAC .018 PERIPHERAL DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020161
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2002
Days to Decision
36 days
Submission Type
Summary

AGILTRAC .018 PERIPHERAL DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020161
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2002
Days to Decision
36 days
Submission Type
Summary