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Thoratec CentriMag Return (Arterial) Cannula Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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