# Abbott (Formerly Thoratec Corporation)

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 2 (2020–2022): 2 510(k) clearances
- Product codes: QNR (1), DWA (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Thoratec Corp: 2 (https://510kreport.com/company/thoratec)
- Thoratec Corporation (Now Part of Abbott): 1 (https://510kreport.com/company/thoratec-now-part-of-abbott)

## Firms that cite its devices most
- Abbott Medical: 2 (https://510kreport.com/company/abbott-medical)

## Its most-cited devices
- K222038: CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support System (2022), cited by 1
- K200306: CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit (2020), cited by 1

## Recent decisions
- K222038: CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support System (Dec 8, 2022)
- K200306: CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit (Mar 6, 2020)

Source page: https://510kreport.com/company/abbott-formerly-thoratec