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Thoratec CentriMag Return (Arterial) Cannula Kit

Page Type
Cleared 510(K)
510(k) Number
K152161
510(k) Type
Special
Applicant
Thoratec Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2015
Days to Decision
46 days
Submission Type
Summary

Thoratec CentriMag Return (Arterial) Cannula Kit

Page Type
Cleared 510(K)
510(k) Number
K152161
510(k) Type
Special
Applicant
Thoratec Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2015
Days to Decision
46 days
Submission Type
Summary