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CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222038
510(k) Type
Traditional
Applicant
Abbott (formerly Thoratec Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2022
Days to Decision
150 days
Submission Type
Summary

CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222038
510(k) Type
Traditional
Applicant
Abbott (formerly Thoratec Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2022
Days to Decision
150 days
Submission Type
Summary