510(k) · Cleared
ClearedCOREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
OrbusNeich Medical (Shenzhen) Co., Ltd. · DQY Catheter, Percutaneous
Cleared on Jan 7, 2025 as substantially equivalent to K231608 (OrbusNeich Medical (Shenzhen) Co., Ltd., 2024) after a 130-day review. Its family tree reaches back 11 generations to 2000.
- Decided
- Jan 7, 2025
- Review
- 130 days
- Class
- Class II
- Product code
- DQY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 11 generations to K001992 (2000). 18 ancestors in all, the oldest K945904 (1995). No later device cites it as a predicate yet.
- Root · 11 generations backK001992 Ilt 0.014 Catheter, Model C114NL2Intra Luminal Therapeutics, Inc. · 2000
- 7 generations between
- 3 generations backK161126 ASAHI Corsair ProAsahi Intecc Co., Ltd. · 2016
- 2 generations backK182360 Teleport MicrocatheterOrbusneich Medical Trading, Inc. · 2018
- 1 generation backK231608 Teleport XT MicrocatheterOrbusNeich Medical (Shenzhen) Co., Ltd. · 2024
- This deviceK242588 COREPASS Modular Microcatheter (FLEX); COREPASS Modular…OrbusNeich Medical (Shenzhen) Co., Ltd. · 2025
Show all 11 generations
- Root · 11 generations backK001992 Ilt 0.014 Catheter, Model C114NL2Intra Luminal Therapeutics, Inc. · 2000
- 10 generations backK012169 Ilt Support Catheter .014, Model C114LW1; Ilt Support Catheter…Intra Luminal Therapeutics, Inc. · 2001
- 9 generations backK030984 Safe Cross Angled Support 0.14, Safe Cross Straight Support Catheter…Intra Luminal Therapeutics, Inc. · 2003
- 8 generations backK032660 Xtrak Support CatheterXtrak Medical, Inc. · 2003
- 7 generations backK051772 Asahi Tornus Support CatheterAsahi Intecc Co., Ltd. · 2005
- 6 generations backK062885 Stride MicrocatheterAsahi Intecc Co., Ltd. · 2007
- 5 generations backK083127 Asahi Corsair MicrocatheterAsahi Intecc Co., Ltd. · 2009
- 4 generations backK151103 ASAHI Corsair MicrocatheterAsahi Intecc Co., Ltd. · 2015
- 3 generations backK161126 ASAHI Corsair ProAsahi Intecc Co., Ltd. · 2016
- 2 generations backK182360 Teleport MicrocatheterOrbusneich Medical Trading, Inc. · 2018
- 1 generation backK231608 Teleport XT MicrocatheterOrbusNeich Medical (Shenzhen) Co., Ltd. · 2024
- This deviceK242588 COREPASS Modular Microcatheter (FLEX); COREPASS Modular…OrbusNeich Medical (Shenzhen) Co., Ltd. · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −11 | K001992 | Ilt 0.014 Catheter, Model C114NL2 | Intra Luminal Therapeutics, Inc. | 2000 | — |
| −10 | K012169 | Ilt Support Catheter .014, Model C114LW1; Ilt Support Catheter Advancing… | Intra Luminal Therapeutics, Inc. | 2001 | — |
| −9 | K030984 | Safe Cross Angled Support 0.14, Safe Cross Straight Support Catheter 0.14… | Intra Luminal Therapeutics, Inc. | 2003 | — |
| −8 | K032660 | Xtrak Support Catheter | Xtrak Medical, Inc. | 2003 | — |
| −7 | K051772 | Asahi Tornus Support Catheter | Asahi Intecc Co., Ltd. | 2005 | — |
| −6 | K062885 | Stride Microcatheter | Asahi Intecc Co., Ltd. | 2007 | — |
| −5 | K083127 | Asahi Corsair Microcatheter | Asahi Intecc Co., Ltd. | 2009 | — |
| −4 | K151103 | ASAHI Corsair Microcatheter | Asahi Intecc Co., Ltd. | 2015 | — |
| −3 | K161126 | ASAHI Corsair Pro | Asahi Intecc Co., Ltd. | 2016 | — |
| −2 | K182360 | Teleport Microcatheter | Orbusneich Medical Trading, Inc. | 2018 | — |
| −1 | K231608 | Teleport XT Microcatheter | OrbusNeich Medical (Shenzhen) Co., Ltd. | 2024 | — |
| 0 (this device) | K242588 | COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL) | OrbusNeich Medical (Shenzhen) Co., Ltd. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 2 | 0 |
| 1996 | 1 | 0 |
| 1997 | 2 | 0 |
| 2000 | 1 | 0 |
| 2005 | 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 DQY? 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 DQY device
- #1 K234115 APRO 55 Catheterscore 17.5 · 6 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 |
|---|---|---|---|
| * | K231608 | Teleport XT MicrocatheterSummary page 5…870.1250) Regulatory Class: II Product Code: DQY Predicate Device: Teleport XT Microcatheter (K231608, DQY, cleared Jan 7, 2024) This predicate has not been subject to a design-related… | 2024 |
| † | K182360 | Teleport Microcatheter | 2018 |
| † | K191560 | Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter | 2019 |
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 25 years and passes through 5 companies; a new generation was cleared every 1.6 years on median.
- None of the 18 ancestors has a recall.
How does its category compare?
All DQY devicesDQY Catheter, Percutaneous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · DQY
21in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DQY
115in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DQY
1in 2025
Class I (10 since 2007) Class II/III not classified
Adverse event reports per year · DQY
3,056in 2025
MAUDE reports naming product code DQY, 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 | 16 | 85 | 6 | 313 |
| 2008 | 31 | 66 | 12 | 496 |
| 2009 | 37 | 73 | 17 | 819 |
| 2010 | 22 | 74 | 32 | 1,293 |
| 2011 | 36 | 71 | 6 | 1,211 |
| 2012 | 30 | 87 | 2 | 1,191 |
| 2013 | 32 | 92 | 36 (1) | 1,352 |
| 2014 | 19 | 127 | 3 | 1,497 |
| 2015 | 27 | 118 | 3 | 2,337 |
| 2016 | 22 | 117 | 22 (7) | 2,252 |
| 2017 | 26 | 113 | 8 | 2,489 |
| 2018 | 25 | 106 | 2 | 2,855 |
| 2019 | 30 | 111 | 1 | 2,902 |
| 2020 | 20 | 120 | 2 | 2,889 |
| 2021 | 18 | 81 | 2 | 3,006 |
| 2022 | 18 | 74 | 0 | 2,643 |
| 2023 | 18 | 114 | 17 | 3,049 |
| 2024 | 16 | 87 | 1 | 3,190 |
| 2025 | 21 | 115 | 1 (1) | 3,056 |
| 2026 | 11 | 30 | 2 (1) | — |
What is it indicated for?
The COREPASS FLEX/CONTROL microcatheters are indicated for:
• supporting and facilitating the placement of guidewires in the coronary and peripheral vasculature (not intended for neurovasculature).
• exchanging guidewires in the coronary and peripheral vasculature.
• the delivery of contrast media into the coronary, peripheral, and abdominal vasculature.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K242588 · printed Nov 3, 2026
Cite this page
510(k) Report. “K242588: COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K242588
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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