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Abbott (Formerly Thoratec Corporation)

FDA Regulatory Profile

Abbott (Formerly Thoratec Corporation) appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 8, 2022.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222038CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support SystemDecember 8, 2022
K200306CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (VMarch 6, 2020

FDA data resources