Last synced on 14 November 2025 at 11:06 pm

AGILTRAC .018 PERIPHERAL DILATATION CATHETER

Page Type
Cleared 510(K)
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)
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