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5F MEDTRONIC LAUNCHER GUIDE CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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