# Thoratec Corp

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 4 (1994–2015): 3 510(k) clearances and 1 original PMA approval
- Names in FDA's records: Thoratec Corp (2); Thoratec Corporation (2)
- Product codes: DWF (2), DSQ (1), DWA (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Levitronix, LLC: 4 (https://510kreport.com/company/levitronix)

## Firms that cite its devices most
- Abbott (Formerly Thoratec Corporation): 2 (https://510kreport.com/company/abbott-formerly-thoratec)

## Its most-cited devices
- K152190: Thoratec CentriMag Drainage (Venous) Cannula Kit (2015), cited by 1
- K152161: Thoratec CentriMag Return (Arterial) Cannula Kit (2015), cited by 1

## Recent decisions
- K152190: Thoratec CentriMag Drainage (Venous) Cannula Kit (Sep 18, 2015)
- K152161: Thoratec CentriMag Return (Arterial) Cannula Kit (Sep 18, 2015)
- K131179: Centrimag Primary Console (2ND Generation); Mag Monitor (Jul 18, 2013)
- P920014: Heartmate VE Lvas (Sep 30, 1994)

Source page: https://510kreport.com/company/thoratec