# K181954: autoLog IQ Autotransfusion System

- Pathway: 510(k) (Special)
- Applicant: Medtronic Perfusion Systems
- Decided: Aug 22, 2018 after 30 days
- Product code: CAC (Apparatus, Autotransfusion)
- Device class: 2
- Regulation: 21 CFR 868.5830
- 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 K972894 (1998). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093535: Autolog Autotransfusion System, Medtronic, Inc. (2010) Summary page 4.

## Indications for use
The autoLog IQ autotransfusion system and Medtronic wash kit are intended for use in the collection, concentration, washing, and reinfusion of autologous blood. Areas of application may include, but are not limited to, the following: • Surgeries including general, cardiovascular, orthopedic, vascular, plastic/reconstructive, obstetric/gynecologic, and neurological • Postoperative treatment areas

Source page: https://510kreport.com/device/K181954
Methodology: https://510kreport.com/methodology