# K093535: Autolog Autotransfusion System

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic, Inc.
- Decided: Mar 22, 2010 after 126 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: 2 generations back to K972894 (1998). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982755: Modification of Autotransfusion Apparatus (Autolog), Medtronic Blood Management (1998) Summary page 1.

## Most influential descendants
- K181954: autoLog IQ Autotransfusion System (2018), 0 descendants of its own

## Indications for use
The autoLog is intended for use in the collection, concentration, washing, and reinfusion of autologous blood. Such areas of application may include, but are not necessarily limited to, the following: * General, Cardiovascular, Orthopedic, Vascular, Plastic/Reconstructive, Obstetric/Gynecologic and Neurosurgical * Postoperative treatment areas

Source page: https://510kreport.com/device/K093535
Methodology: https://510kreport.com/methodology