# K070286: Bio-Console, Model 560

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic
- Decided: May 22, 2007 after 113 days
- Product code: DWA (Control, Pump Speed, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4380
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K915183 (1992). 10 ancestors in all.
6 later devices descend from it; 3 cite it directly.
1 of 17 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051303: Bio-Console, Model 560, Medtronic Perfusion Systems (2005)
- K022947: Advanced Perfusion System 1 (100/120 Volt),Advanced Perfusion System 1 (220/240 Volt, Roller Pumps (6, 4 Inch, Terumo Cardiovascular Systems Corp. (2003) Summary page 1.
- K961364: Automatic Tubing Clamp System (Atc), Rocky Mountain Research, Inc. (1996) Summary page 1.

## Most influential descendants
- K080824: Bio-Console 560 (2008), 3 descendants of its own
- K131964: Bio-Console 560 Extracorporeal Blood Pumping Console (2013), 2 descendants of its own
- K221491: Anivia SG1000 Pump Console (2023), 1 descendant of its own
- K230698: Anivia SG1000 Pump Console (2023), 0 descendants of its own
- K150530: Level Sensor, Level Sensor Tape (2015), 0 descendants of its own

## Indications for use
The Medtronic centrifugal blood pumping system is intended to pump blood through the extracorporeal bypass circuit for extracorporeal support for periods appropriate to cardiopulmonary bypass procedures (up to 6 hours).

Source page: https://510kreport.com/device/K070286
Methodology: https://510kreport.com/methodology