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DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITHOUT PRESSURE MONITORING LINE, DLP RETROGRADE CORONARY SINUS PERFUSIO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132995
510(k) Type
Special
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2013
Days to Decision
37 days
Submission Type
Summary

DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITHOUT PRESSURE MONITORING LINE, DLP RETROGRADE CORONARY SINUS PERFUSIO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132995
510(k) Type
Special
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2013
Days to Decision
37 days
Submission Type
Summary