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5F MEDTRONIC LAUNCHER GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K030779
510(k) Type
Special
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2003
Days to Decision
44 days
Submission Type
Summary

5F MEDTRONIC LAUNCHER GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K030779
510(k) Type
Special
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2003
Days to Decision
44 days
Submission Type
Summary