510(k) · Cleared
ClearedAngiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Possis Medical, Inc. · QEZ Aspiration Thrombectomy Catheter
Cleared on Aug 24, 2007 as substantially equivalent to K040013 (Possis Medical, Inc., 2004) and 2 other predicates after a 105-day review. Its family tree reaches back 6 generations to 1990. 1 of the 44 devices in its family, counting itself, has a Class I recall. 33 later devices descend from it.
- Decided
- Aug 24, 2007
- Review
- 105 days
- Class
- Class II
- Product code
- QEZ
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 6 generations to K901627 (1990). 10 ancestors in all, the oldest K780551 (1978). 33 later devices descend from it, 1 citing it directly. 1 of the 44 devices in this family, counting this one, has a Class I recall.
- Root · 6 generations backK901627 Arterial Embolectomy CatheterApplied Vascular Devices, Inc. · 1990 · Recalled
- 5 generations backK960970 Possis Angiojet Rapid Thrombectomy Catheter System, F105…Possis Medical, Inc. · 1996
- 4 generations backK972610 Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model…Possis Medical, Inc. · 2000
- 3 generations backK040013 Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray…Possis Medical, Inc. · 2004
- 2 generations backK052256 Angiojet Xpeedior 120 CatheterPossis Medical, Inc. · 2005
- 1 generation backK061951 Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model Xpeedior 120Possis Medical, Inc. · 2006
- This deviceK071336 Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307Possis Medical, Inc. · 2007
- Descendant · cites it directly · 32 of its ownK090253 Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet…Possis Medical, Inc. · 2009
- Descendant · 2 generations on · 31 of its ownK091593 Angio Jet Ultra DVX and Xpeedior Thrombectomy SetsPossis Medical, Inc. · 2009
- Descendant · 3 generations on · 30 of its ownK101406 Angiojet Solent Proxi Thrombectomy Set Model 109676-001Medrad Interventional/Possis · 2010
- Descendant · 3 generations on · 28 of its ownK111182 Angiojet Solent Omni Thrombectomy SetMedrad, Inc. · 2011 · Recalled
- Descendant · 4 generations on · 26 of its ownK151313 ZelanteDVT Thrombectomy SetBoston Scientific Corporation · 2015
Showing 5 of 33 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K223210 ClotTriever XL Catheter9 generations on · 2023
Most influential descendants
Showing 5 of 33 · See all- K090253Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior…Possis Medical, Inc. · 2009 · cites it directly32descendants
- K091593Angio Jet Ultra DVX and Xpeedior Thrombectomy SetsPossis Medical, Inc. · 2009 · 2 generations on31descendants
- K101406Angiojet Solent Proxi Thrombectomy Set Model 109676-001Medrad Interventional/Possis · 2010 · 3 generations on30descendants
- K111182Angiojet Solent Omni Thrombectomy SetMedrad, Inc. · 2011 · 3 generations on28descendants
- K151313ZelanteDVT Thrombectomy SetBoston Scientific Corporation · 2015 · 4 generations on26descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K901627 | Arterial Embolectomy Catheter | Applied Vascular Devices, Inc. | 1990 | 1 |
| −5 | K960970 | Possis Angiojet Rapid Thrombectomy Catheter System, F105 Catheter,Model… | Possis Medical, Inc. | 1996 | — |
| −4 | K972610 | Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model 3030C, LF140… | Possis Medical, Inc. | 2000 | — |
| −3 | K040013 | Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray Ancillary Kit | Possis Medical, Inc. | 2004 | — |
| −2 | K052256 | Angiojet Xpeedior 120 Catheter | Possis Medical, Inc. | 2005 | — |
| −1 | K061951 | Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model Xpeedior 120 | Possis Medical, Inc. | 2006 | — |
| 0 (this device) | K071336 | Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307 | Possis Medical, Inc. | 2007 | — |
| +1 | K090253 | Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior… | Possis Medical, Inc. | 2009 | — |
| +2 | K091593 | Angio Jet Ultra DVX and Xpeedior Thrombectomy Sets | Possis Medical, Inc. | 2009 | — |
| +3 | K101406 | Angiojet Solent Proxi Thrombectomy Set Model 109676-001 | Medrad Interventional/Possis | 2010 | — |
| +3 | K111182 | Angiojet Solent Omni Thrombectomy Set | Medrad, Inc. | 2011 | 1 |
| +4 | K151313 | ZelanteDVT Thrombectomy Set | Boston Scientific Corporation | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1978 | 1 | 0 |
| 1991 | 1 | 0 |
| 1995 | 1 | 0 |
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 2 | 0 |
| 2010 | 1 | 0 |
| 2011 | 2 | 0 |
| 2012 | 1 | 0 |
| 2015 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 3 | 0 |
| 2022 | 2 | 0 |
| 2023 | 9 | 1 |
| 2024 | 3 | 0 |
| 2025 | 4 | 0 |
| 2026 | 3 | 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.
1 device in this family has a Class I recall. 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? (3)
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 |
|---|---|---|---|
| * | K040013 | Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray Ancillary KitSummary page 5…ame: XPEEDIOR™ Rheolytic Thrombectomy Catheter Device Classification Name: Embolectomy Catheter Predicate Devices: AngioJet XPEEDIOR® Rheolytic™ Thrombectomy Catheter (K040013, K052256 and K061951) Device Description When used with the Angiolet System, the XPEEDIOR Rheolytic Thrombectomy Catheter uses… | 2004 |
| * | K052256 | Angiojet Xpeedior 120 CatheterSummary page 5…DIOR™ Rheolytic Thrombectomy Catheter Device Classification Name: Embolectomy Catheter Predicate Devices: AngioJet XPEEDIOR® Rheolytic™ Thrombectomy Catheter (K040013, K052256 and K061951) Device Description When used with the Angiolet System, the XPEEDIOR Rheolytic Thrombectomy Catheter uses high velo… | 2005 |
| * | K061951 | Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model Xpeedior 120Summary page 5…tic Thrombectomy Catheter Device Classification Name: Embolectomy Catheter Predicate Devices: AngioJet XPEEDIOR® Rheolytic™ Thrombectomy Catheter (K040013, K052256 and K061951) Device Description When used with the Angiolet System, the XPEEDIOR Rheolytic Thrombectomy Catheter uses high velocity saline… | 2006 |
What descends from it? (33)
See all 331 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K090253 | Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior… | 2009 | 32 |
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K223210ClotTriever XL CatheterInari Medical, Inc. · 2023 · 9 generations on · ◆ in the 2023 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 17 years and passes through 2 companies; a new generation was cleared every 3.4 years on median.
- 4 of the 10 ancestors have a recall of any class.
- Of its descendants, K090253 (Possis Medical, Inc., 2009) has gone furthest, with 32 descendants of its own.
- 4 other devices also cite its predicate K040013.
How does its category compare?
All QEZ devicesQEZ Aspiration Thrombectomy Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, 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?
The AngioJet XPEEDIOR 120 Rheolytic Thrombectomy Catheter is intended for use with the AngioJet System in breaking apart and removing thrombus from:
· infra-inguinal peripheral arteries > 3.0 mm in diameter,
* upper extremity peripheral veins > 3.0 mm in diameter and
* ileofemoral and lower extremity veins > 3.0 mm in diameter.
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/K071336 · printed Nov 4, 2026
Cite this page
510(k) Report. “K071336: Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071336
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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