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MEDTRONIC RESTING HEART SYSTEM, MODEL AAR1000 AND 711

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031700
510(k) Type
Traditional
Applicant
Medtronic Perfusion Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2003
Days to Decision
88 days
Submission Type
Summary

MEDTRONIC RESTING HEART SYSTEM, MODEL AAR1000 AND 711

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031700
510(k) Type
Traditional
Applicant
Medtronic Perfusion Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2003
Days to Decision
88 days
Submission Type
Summary