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7F LAUNCHER GUIDE CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022764
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2002
Days to Decision
7 days
Submission Type
Summary

7F LAUNCHER GUIDE CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022764
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2002
Days to Decision
7 days
Submission Type
Summary