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6F Z4 GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K042489
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2004
Days to Decision
90 days
Submission Type
Summary

6F Z4 GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K042489
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2004
Days to Decision
90 days
Submission Type
Summary