510(k) Report

510(k) · Cleared

Cleared

EndoWave Infusion System

K080392510(k) SpecialCleared Apr 30, 200877-day reviewClass II21 CFR 870.5150

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Ekos Corp. · QEY Mechanical Thrombolysis Catheter

Cleared on Apr 30, 2008 as substantially equivalent to K072507 (Ekos Corp., 2007) and 1 other predicate after a 77-day review. Its family tree reaches back 14 generations to 1990. 11 later devices descend from it.

Decided
Apr 30, 2008
Review
77 days
Class
Class II
Product code
QEY
Recalls
None
Predicates
2

Its longest line of descent runs back 14 generations to K904788 (1990). 36 ancestors in all. 11 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2006: 1 other ancestor2005: 4 other ancestors2003: 2 other ancestors2001: 1 other ancestor2000: 2 other ancestors1996: 2 other ancestors1993: 3 other ancestors1995: 1 other ancestor1999: 2 other ancestors1997: 1 other ancestor1994: 1 other ancestor1991: 1 other ancestor2008: 1 descendant cleared2011: 1 descendant cleared2019: 3 descendants cleared2021: 1 descendant cleared2024: 1 descendant cleared2020: 2 descendants cleared2026: 2 descendants clearedK904788 · Mewissen Catheter · Boston Scientific Corp · 1990K974067 · Fountain Infusion Catheter and Occluding Guide Wire · Merit Medical Systems, Inc. · 1998 · recalledK981417 · Squirt Fluid Delivery System · Merit Medical Systems, Inc. · 1998K013635 · Trellis Infusion System (10CM Infusion Length); Trellis Infusion System (20CM Infusion Length) · Bacchus Vascular, Inc. · 2002K021958 · Trellis Plus Infusion System (140CM Catheter Length 10CM Infusion Length 20CM (100CM Catheter Length 10CM Infusion H · Bacchus Vascular, Inc. · 2002 · recalledK023514 · Trellis-6 Peripheral Infusion System (140CM Catheter Length 10CM Infusion Length) · Bacchus Vascular, Inc. · 2002 · recalled×2: 2 generations cleared close together, K030637 (2003), K033214 (2003) ×2: 2 generations cleared close together, K041629 (2004), K042456 (2004) ×2: 2 generations cleared close together, K051319 (2005), K052071 (2005) K060084 · Lysus Infusion System · Ekos Corp. · 2006K062508 · Neurowave Micro-Infusion System · Ekos Corp. · 20061990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 2 other ancestors4 generations back: 1 other ancestor5 generations back: 6 other ancestors6 generations back: 2 other ancestors7 generations back: 4 other ancestors8 generations back: 4 other ancestors 1 generation forward: 1 descendant2 generations forward: 1 descendant3 generations forward: 1 descendant4 generations forward: 5 descendants5 generations forward: 2 descendants6 generations forward: 1 descendant K062508 · Neurowave Micro-Infusion System · Ekos Corp. · 2006K060084 · Lysus Infusion System · Ekos Corp. · 2006K052071 · Lysus Infusion System · Ekos Corp. · 2005K051319 · Lysus Infusion System · Ekos Corp. · 2005K042456 · Lysus Infusion System · Ekos Corp. · 2004 · recalledK041629 · Lysus Infusion System · Ekos Corp. · 2004K033214 · Ekos Peripheral Infusion System · Ekos Corp. · 2003K030637 · Ekos Peripheral Infusion System · Ekos Corp. · 2003K023514 · Trellis-6 Peripheral Infusion System (140CM Catheter Length 10CM Infusion Length) · Bacchus Vascular, Inc. · 2002 · recalledK021958 · Trellis Plus Infusion System (140CM Catheter Length 10CM Infusion Length 20CM (100CM Catheter Length 10CM Infusion H · Bacchus Vascular, Inc. · 2002 · recalledK013635 · Trellis Infusion System (10CM Infusion Length); Trellis Infusion System (20CM Infusion Length) · Bacchus Vascular, Inc. · 2002K981417 · Squirt Fluid Delivery System · Merit Medical Systems, Inc. · 1998K974067 · Fountain Infusion Catheter and Occluding Guide Wire · Merit Medical Systems, Inc. · 1998 · recalledK904788 · Mewissen Catheter · Boston Scientific Corp · 1990−10−50+5
  1. Root · 14 generations backK904788 Mewissen CatheterBoston Scientific Corp · 1990
  2. 10 generations between
  3. 3 generations backK052071 Lysus Infusion SystemEkos Corp. · 2005
  4. 2 generations backK060084 Lysus Infusion SystemEkos Corp. · 2006
  5. 1 generation backK062508 Neurowave Micro-Infusion SystemEkos Corp. · 2006
  6. This deviceK080392 EndoWave Infusion SystemEkos Corp. · 2008
  7. Descendant · cites it directly · 10 of its ownK081467 Ekosonic Endovascular System with Rapid Pulse ModulationEkos Corp. · 2008 · Recalled
  8. Descendant · 2 generations on · 9 of its ownK111705 Ekosonic Endovascular SystemEkos Corporation · 2011 · Recalled
  9. Descendant · 3 generations on · 8 of its ownK183290 Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular…Thrombolex, Inc. · 2019
  10. Descendant · 4 generations on · 2 of its ownK192864 UNI*FUSE Infusion System with Cooper WireAngioDynamics, Inc. · 2020
  11. Descendant · 4 generations on · 1 of its ownK241851 Versus™ Catheter (VS110-8B)Liquet Medical, Inc. · 2024
Show all 14 generations
  1. Root · 14 generations backK904788 Mewissen CatheterBoston Scientific Corp · 1990
  2. 13 generations backK974067 Fountain Infusion Catheter and Occluding Guide WireMerit Medical Systems, Inc. · 1998 · Recalled
  3. 12 generations backK981417 Squirt Fluid Delivery SystemMerit Medical Systems, Inc. · 1998
  4. 11 generations backK013635 Trellis Infusion System (10CM Infusion Length); Trellis Infusion…Bacchus Vascular, Inc. · 2002
  5. 10 generations backK021958 Trellis Plus Infusion System (140CM Catheter Length 10CM Infusion…Bacchus Vascular, Inc. · 2002 · Recalled
  6. 9 generations backK023514 Trellis-6 Peripheral Infusion System (140CM Catheter Length 10CM…Bacchus Vascular, Inc. · 2002 · Recalled
  7. 8 generations backK030637 Ekos Peripheral Infusion SystemEkos Corp. · 2003
  8. 7 generations backK033214 Ekos Peripheral Infusion SystemEkos Corp. · 2003
  9. 6 generations backK041629 Lysus Infusion SystemEkos Corp. · 2004
  10. 5 generations backK042456 Lysus Infusion SystemEkos Corp. · 2004 · Recalled
  11. 4 generations backK051319 Lysus Infusion SystemEkos Corp. · 2005
  12. 3 generations backK052071 Lysus Infusion SystemEkos Corp. · 2005
  13. 2 generations backK060084 Lysus Infusion SystemEkos Corp. · 2006
  14. 1 generation backK062508 Neurowave Micro-Infusion SystemEkos Corp. · 2006
  15. This deviceK080392 EndoWave Infusion SystemEkos Corp. · 2008

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2008: 12011: 12019: 32020: 22021: 12024: 12026: 2
2008high 3 (2019) · low 0 (2009)2026

Most influential descendants

Showing 5 of 11 · See all
  • K081467Ekosonic Endovascular System with Rapid Pulse ModulationEkos Corp. · 2008 · cites it directly10descendants
  • K111705Ekosonic Endovascular SystemEkos Corporation · 2011 · 2 generations on9descendants
  • K183290Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200Thrombolex, Inc. · 2019 · 3 generations on8descendants
  • K192864UNI*FUSE Infusion System with Cooper WireAngioDynamics, Inc. · 2020 · 4 generations on2descendants
  • K241851Versus™ Catheter (VS110-8B)Liquet Medical, Inc. · 2024 · 4 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−14K904788Mewissen CatheterBoston Scientific Corp1990—
−13K974067Fountain Infusion Catheter and Occluding Guide WireMerit Medical Systems, Inc.199823
−12K981417Squirt Fluid Delivery SystemMerit Medical Systems, Inc.1998—
−11K013635Trellis Infusion System (10CM Infusion Length); Trellis Infusion System (20CM…Bacchus Vascular, Inc.2002—
−10K021958Trellis Plus Infusion System (140CM Catheter Length 10CM Infusion Length 20CM…Bacchus Vascular, Inc.20021
−9K023514Trellis-6 Peripheral Infusion System (140CM Catheter Length 10CM Infusion…Bacchus Vascular, Inc.20021
−8K030637Ekos Peripheral Infusion SystemEkos Corp.2003—
−7K033214Ekos Peripheral Infusion SystemEkos Corp.2003—
−6K041629Lysus Infusion SystemEkos Corp.2004—
−5K042456Lysus Infusion SystemEkos Corp.20043
−4K051319Lysus Infusion SystemEkos Corp.2005—
−3K052071Lysus Infusion SystemEkos Corp.2005—
−2K060084Lysus Infusion SystemEkos Corp.2006—
−1K062508Neurowave Micro-Infusion SystemEkos Corp.2006—
0 (this device)K080392EndoWave Infusion SystemEkos Corp.2008—
+1K081467Ekosonic Endovascular System with Rapid Pulse ModulationEkos Corp.20085
+2K111705Ekosonic Endovascular SystemEkos Corporation20115
+3K183290Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter…Thrombolex, Inc.2019—
+4K192864UNI*FUSE Infusion System with Cooper WireAngioDynamics, Inc.2020—
+4K241851Versus™ Catheter (VS110-8B)Liquet Medical, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199330
199410
199510
199620
199710
199920
200020
200110
200320
200540
200610
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
201110
201930
202020
202110
202410
202620
FIG. 1 — Lineage of K080392, 1990–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 QEY? 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 QEY device

  1. #1 K241851 Versus™ Catheter (VS110-8B)score 16.8 · 19 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K072507Endowave Infusion System
Summary page 1
…ry Name: Endo Wave Infusion System Name of Predicate Device: EndoWave Infusion System 5 10O(k) Reference No.: K072507, K062508 Device Description The system consists of a disposable infusion catheter with removable ultrasound core and an instrume…
Ekos Corp.20073
*K062508Neurowave Micro-Infusion System
Summary page 1
…Endo Wave Infusion System Name of Predicate Device: EndoWave Infusion System 5 10O(k) Reference No.: K072507, K062508 Device Description The system consists of a disposable infusion catheter with removable ultrasound core and an instrument that g…
Ekos Corp.2006—

Also cleared against K072507: 1 other device →

What descends from it? (11)

See all 11

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K081467Ekosonic Endovascular System with Rapid Pulse ModulationEkos Corp.200810

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 18 years and passes through 4 companies; a new generation was cleared every 8 months on median.
  • 9 of the 36 ancestors have a recall of any class.
  • Of its descendants, K081467 (Ekos Corp., 2008) has gone furthest, with 10 descendants of its own.
  • 1 other device also cites its predicate K072507.

How does its category compare?

All QEY devices

QEY Mechanical Thrombolysis Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · QEY

1in 2024

2007: 52008: 42011: 12013: 12014: 12015: 12016: 22017: 32018: 12019: 52020: 32021: 32022: 12023: 22024: 12026 (partial year): 2
2007high 5 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QEY

62in 2021

2007: 28 days median2008: 54 days median2017: 144 days median2019: 91 days median2020: 158 days median2021: 62 days median
2007high 158 (2020) · low 28 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · QEY

1in 2023

2022: 12023: 1
2007high 1 (2022) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · QEY

5in 2025

2023: 12024: 12025: 5
2007high 5 (2025) · low 0 (2007)2025

MAUDE reports naming product code QEY, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200752800
200845400
20090—00
20100—00
20111—00
20120—00
20131—00
20141—00
20151—00
20162—00
2017314400
20181—00
201959100
2020315800
202136200
20221—10
20232—11
20241—01
20250—05
20262—0—

What is it indicated for?

The Endo Wave Infusion System is intended for the controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K080392: EndoWave Infusion System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K080392

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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