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5F GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K000598
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2000
Days to Decision
30 days
Submission Type
Summary

5F GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K000598
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2000
Days to Decision
30 days
Submission Type
Summary