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DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123762
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2013
Days to Decision
110 days
Submission Type
Summary

DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123762
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2013
Days to Decision
110 days
Submission Type
Summary