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CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200306
510(k) Type
Special
Applicant
Abbott (formerly Thoratec Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2020
Days to Decision
29 days
Submission Type
Summary

CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200306
510(k) Type
Special
Applicant
Abbott (formerly Thoratec Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2020
Days to Decision
29 days
Submission Type
Summary