# K152190: Thoratec CentriMag Drainage (Venous) Cannula Kit

- Pathway: 510(k) (Special)
- Applicant: Thoratec Corporation
- Decided: Sep 18, 2015 after 44 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K870109 (1987). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110983: Centrimag Drainage Cannula Kit, Levitronix, LLC (2011) Summary page 4.

## Most influential descendants
- K200306: CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit (2020), 1 descendant of its own
- K234118: CentriMag™ Acute Circulatory Support System (2024), 0 descendants of its own

## Indications for use
The CentriMag Drainage (Venous) Cannula is indicated for use with an extracorporeal bypass circuit for extracorporeal circulatory support for periods up to six hours.

Source page: https://510kreport.com/device/K152190
Methodology: https://510kreport.com/methodology