510(k) · Cleared
ClearedautoLog IQ Autotransfusion System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtronic Perfusion Systems · CAC Apparatus, Autotransfusion
Cleared on Aug 22, 2018 as substantially equivalent to K093535 (Medtronic, Inc., 2010) after a 30-day review. Its family tree reaches back 3 generations to 1998.
- Decided
- Aug 22, 2018
- Review
- 30 days
- Class
- Class II
- Product code
- CAC
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K972894 (1998). No later device cites it as a predicate yet.
- Root · 3 generations backK972894 Autotransfusion Appartus (Autolog)Medtronic Blood Management · 1998 · Recalled
- 2 generations backK982755 Modification of Autotransfusion Apparatus (Autolog)Medtronic Blood Management · 1998
- 1 generation backK093535 Autolog Autotransfusion SystemMedtronic, Inc. · 2010
- This deviceK181954 autoLog IQ Autotransfusion SystemMedtronic Perfusion Systems · 2018
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K972894 | Autotransfusion Appartus (Autolog) | Medtronic Blood Management | 1998 | 1 |
| −2 | K982755 | Modification of Autotransfusion Apparatus (Autolog) | Medtronic Blood Management | 1998 | — |
| −1 | K093535 | Autolog Autotransfusion System | Medtronic, Inc. | 2010 | — |
| 0 (this device) | K181954 | autoLog IQ Autotransfusion System | Medtronic Perfusion Systems | 2018 | — |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in CAC? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new CAC device
- #1 K240426 Aventus Clot Management Systemscore 11.2 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K093535 | Autolog Autotransfusion SystemSummary page 4…ial controls or performance standards have been established for these devices. Name of Predicate Device: autoLog Autotransfusion System, 510(k) K093535 K181954 510(k) Summary Page 1 Device Description The autoLog IQ Autotransfusion System is used to collect autol… | 2010 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 20 years and passes through 3 companies; a new generation was cleared every 8.4 years on median.
- 1 of the 3 ancestors has a recall of any class.
How does its category compare?
All CAC devicesCAC Apparatus, Autotransfusion: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.
FDA decisions per year · CAC
3in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · CAC
91in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · CAC
7in 2023
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · CAC
128in 2025
MAUDE reports naming product code CAC, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 1 | 35 |
| 2008 | 1 | — | 5 | 12 |
| 2009 | 0 | — | 25 | 68 |
| 2010 | 4 | 123 | 3 | 115 |
| 2011 | 2 | — | 3 | 939 |
| 2012 | 3 | 90 | 0 | 249 |
| 2013 | 1 | — | 9 | 153 |
| 2014 | 3 | 269 | 0 | 90 |
| 2015 | 0 | — | 0 | 87 |
| 2016 | 2 | — | 0 | 73 |
| 2017 | 1 | — | 2 | 88 |
| 2018 | 2 | — | 2 | 87 |
| 2019 | 1 | — | 23 | 64 |
| 2020 | 1 | — | 0 | 108 |
| 2021 | 4 | 155 | 0 | 73 |
| 2022 | 1 | — | 0 | 65 |
| 2023 | 2 | — | 7 (2) | 39 |
| 2024 | 3 | 91 | 0 | 129 |
| 2025 | 0 | — | 0 | 128 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
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
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K181954 · printed Nov 6, 2026
Cite this page
510(k) Report. “K181954: autoLog IQ Autotransfusion System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K181954
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026