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MEDTRONIC SHERPA GUIDING CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955651
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1996
Days to Decision
41 days
Submission Type
Summary

MEDTRONIC SHERPA GUIDING CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955651
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1996
Days to Decision
41 days
Submission Type
Summary