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EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061254
510(k) Type
Special
Applicant
Medtronic Perfusion Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2006
Days to Decision
50 days
Submission Type
Summary

EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061254
510(k) Type
Special
Applicant
Medtronic Perfusion Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2006
Days to Decision
50 days
Submission Type
Summary