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DLP CORONARY OSTIAL PERFUSION CANNULAE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131269
510(k) Type
Special
Applicant
MEDTRONIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2013
Days to Decision
68 days
Submission Type
Summary

DLP CORONARY OSTIAL PERFUSION CANNULAE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131269
510(k) Type
Special
Applicant
MEDTRONIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2013
Days to Decision
68 days
Submission Type
Summary