510(k) · Cleared
ClearedExport XT Catheter, Export AP Catheter
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtronic, Inc. · QEZ Aspiration Thrombectomy Catheter
Cleared on Jun 7, 2012 as substantially equivalent to K061958 (Medtronic Vascular, 2006) and 1 other predicate after an 83-day review. Its family tree reaches back 5 generations to 2001. 5 later devices descend from it.
- Decided
- Jun 7, 2012
- Review
- 83 days
- Class
- Class II
- Product code
- QEZ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 5 generations to K010579 (2001). 9 ancestors in all. 5 later devices descend from it, 1 citing it directly.
- Root · 5 generations backK010579 Stent Support Guide CatheterMedtronic Vascular · 2001 · Recalled
- 4 generations backK030201 Modification to Export Aspiration CatheterMedtronic Vascular · 2003
- 3 generations backK040869 Export CatheterMedtronic Vascular · 2004
- 2 generations backK061958 Medtronic Export XT CatheterMedtronic Vascular · 2006 · Recalled
- 1 generation backK081573 Medtronic Export AP CatheterMedtronic Vascular · 2008
- This deviceK120808 Export XT Catheter, Export AP CatheterMedtronic, Inc. · 2012
- Descendant · cites it directly · 4 of its ownK130536 Export Advance Aspiration CatheterMedtronic, Inc. · 2013
- Descendant · 2 generations on · 2 of its ownK152335 Export Advance Aspiration CatheterMedtronic, Inc. · 2015
- Descendant · 2 generations on · 0 of its ownK253589 Liberant™ RX Aspiration CatheterMedtronic Interventional Vascular, Inc. · 2026
- Descendant · 3 generations on · 0 of its ownK190619 Aspiron (TM) Aspiration CatheterMeril Life Sciences Private Limited · 2019
- Descendant · 2 generations on · 0 of its ownK163031 Bunegin-Albin Air Aspiration SetCook Incorporated · 2017
Most influential descendants
Showing 5 of 5 · See all- K130536Export Advance Aspiration CatheterMedtronic, Inc. · 2013 · cites it directly4descendants
- K152335Export Advance Aspiration CatheterMedtronic, Inc. · 2015 · 2 generations on2descendants
- K253589Liberant™ RX Aspiration CatheterMedtronic Interventional Vascular, Inc. · 2026 · 2 generations on0descendants
- K190619Aspiron (TM) Aspiration CatheterMeril Life Sciences Private Limited · 2019 · 3 generations on0descendants
- K163031Bunegin-Albin Air Aspiration SetCook Incorporated · 2017 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K010579 | Stent Support Guide Catheter | Medtronic Vascular | 2001 | 27 |
| −4 | K030201 | Modification to Export Aspiration Catheter | Medtronic Vascular | 2003 | — |
| −3 | K040869 | Export Catheter | Medtronic Vascular | 2004 | — |
| −2 | K061958 | Medtronic Export XT Catheter | Medtronic Vascular | 2006 | 1 |
| −1 | K081573 | Medtronic Export AP Catheter | Medtronic Vascular | 2008 | — |
| 0 (this device) | K120808 | Export XT Catheter, Export AP Catheter | Medtronic, Inc. | 2012 | — |
| +1 | K130536 | Export Advance Aspiration Catheter | Medtronic, Inc. | 2013 | — |
| +2 | K152335 | Export Advance Aspiration Catheter | Medtronic, Inc. | 2015 | — |
| +2 | K253589 | Liberant™ RX Aspiration Catheter | Medtronic Interventional Vascular, Inc. | 2026 | — |
| +3 | K190619 | Aspiron (TM) Aspiration Catheter | Meril Life Sciences Private Limited | 2019 | — |
| +2 | K163031 | Bunegin-Albin Air Aspiration Set | Cook Incorporated | 2017 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 3 | 0 |
| 2003 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2015 | 1 | 0 |
| 2017 | 1 | 0 |
| 2019 | 1 | 0 |
| 2026 | 1 | 0 |
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 QEZ? 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 QEZ device
- #1 K253925 Aventus Thrombectomy Systemscore 17.9 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K061958 | Medtronic Export XT CatheterSummary page 6…Name: Percutaneous Catheter Classification Embolectomy Catheter Name: Class II per 21 CFR 870.5150, Product Code DXE Predicate Devices: K06195 8 - Medtronic Vascular Export® XT Catheter K081573 - Medtronic Vascular Export® AP Catheter Device… | 2006 |
| * | K081573 | Medtronic Export AP CatheterSummary page 6…Catheter Name: Class II per 21 CFR 870.5150, Product Code DXE Predicate Devices: K06195 8 - Medtronic Vascular Export® XT Catheter K081573 - Medtronic Vascular Export® AP Catheter Device The Export XT & Export AP Catheters are dual lumen catheters Descr… | 2008 |
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K130536 | Export Advance Aspiration Catheter | 2013 | 4 |
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 11 years and passes through 2 companies; a new generation was cleared every 1.8 years on median.
- 3 of the 9 ancestors have a recall of any class.
- Of its descendants, K130536 (Medtronic, Inc., 2013) has gone furthest, with 4 descendants of its own.
- 6 other devices also cite its predicate K061958.
How does its category compare?
All QEZ devicesQEZ Aspiration Thrombectomy Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · QEZ
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · QEZ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · QEZ
No recall names QEZ since 2007.
Adverse event reports per year · QEZ
21in 2025
MAUDE reports naming product code QEZ, 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 | 11 | 79 | 0 | 0 |
| 2008 | 6 | 72 | 0 | 0 |
| 2009 | 4 | 83 | 0 | 0 |
| 2010 | 3 | 33 | 0 | 0 |
| 2011 | 7 | 118 | 0 | 0 |
| 2012 | 5 | 90 | 0 | 0 |
| 2013 | 4 | 144 | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 3 | 112 | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 3 | 94 | 0 | 0 |
| 2020 | 3 | 120 | 0 | 0 |
| 2021 | 3 | 53 | 0 | 2 |
| 2022 | 2 | — | 0 | 18 |
| 2023 | 1 | — | 0 | 14 |
| 2024 | 1 | — | 0 | 17 |
| 2025 | 5 | 108 | 0 | 21 |
| 2026 | 6 | 98 | 0 | — |
What is it indicated for?
- Removal/aspiration of embolic material (thrombus/debris) from vessels of the arterial system, and
- To sub selectively infuse/deliver diagnostics or therapeutics agents with or without vessel occlusion.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K120808 · printed Nov 6, 2026
Cite this page
510(k) Report. “K120808: Export XT Catheter, Export AP Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K120808
Report an extraction error
Are you the manufacturer?
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