Abbott (Formerly Thoratec Corporation) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Abbott (Formerly Thoratec Corporation) - FDA 510(k) Cleared Devices
Recent clearances: CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support System, CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit
2
Total
2
Cleared
0
Denied
Abbott (Formerly Thoratec Corporation) has 2 FDA 510(k) cleared medical devices. Based in Pleasnaton, US.
Last cleared in 2022. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Abbott (Formerly Thoratec Corporation) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Abbott (Formerly Thoratec Corporation)
2 devices