510(k) · Cleared
Recalled · Class II · 2025Modification to Envoy and Vista Brite Tip
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cordis Corp. · DQY Catheter, Percutaneous
Cleared on Jun 13, 2002 after a 29-day review. The FDA summary names its predicate without a number. 3 later devices descend from it. It has been recalled 3 times.
- Decided
- Jun 13, 2002
- Review
- 29 days
- Class
- Class II
- Product code
- DQY
- Recalls
- 3
- Predicates
- 0
3 later devices descend from it, 1 citing it directly.
- This deviceK021593 Modification to Envoy and Vista Brite TipCordis Corp. · 2002
- Descendant · cites it directly · 2 of its ownK082143 Micro Guide Catheter XPCordis Corp. · 2008
- Descendant · 2 generations on · 1 of its ownK140438 Micro Guide Catheter EliteCordis Corp., A Johnson & Johnson Co. · 2014
- Descendant · 3 generations on · 0 of its ownK150187 ELITECROSS Support CatheterCordis Corporation, A Johnson & Johnson Company · 2015
Most influential descendants
Showing 3 of 3 · See all- K082143Micro Guide Catheter XPCordis Corp. · 2008 · cites it directly2descendants
- K140438Micro Guide Catheter EliteCordis Corp., A Johnson & Johnson Co. · 2014 · 2 generations on1descendant
- K150187ELITECROSS Support CatheterCordis Corporation, A Johnson & Johnson Company · 2015 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K021593 | Modification to Envoy and Vista Brite Tip | Cordis Corp. | 2002 | — |
| +1 | K082143 | Micro Guide Catheter XP | Cordis Corp. | 2008 | — |
| +2 | K140438 | Micro Guide Catheter Elite | Cordis Corp., A Johnson & Johnson Co. | 2014 | — |
| +3 | K150187 | ELITECROSS Support Catheter | Cordis Corporation, A Johnson & Johnson Company | 2015 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
| 2014 | 1 | 0 |
| 2015 | 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? (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 |
|---|---|---|---|
| * | — | Cordis Vista Brite Tip Guiding Catheters Named without a submission number | |
| * | — | Cordis Envoy Guiding Catheters Named without a submission number |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K082143 | Micro Guide Catheter XP | 2008 | 2 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Feb 7, 2025 | Class II | Z-1330-2025 | Employee error | Catheter manufactured at the incorrect length. |
| Feb 7, 2019 | Class III | Z-1198-2019 | Equipment maintenance | Frayed pieces of the mounting card being inside the primary packaging. |
| Dec 7, 2004 | Not classified | Z-0434-05 | Other | Two complaints have been received and confirmed, regarding a lot, indicating that the distal end had an 'RDC' shape rather than the 'RDC(1)' shape. The RDC shape has a larger curve. The product was manufactured with the incorrect forming… |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K082143 (Cordis Corp., 2008) has gone furthest, with 2 descendants of its own.
How does its category compare?
All DQY devicesDQY Catheter, Percutaneous: FDA decisions, review times, recalls and adverse event reports over 20 years.
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?
Vista Brite Tip - The guiding catheter is intended for use for intravascular introduction of interventional / diagnostic devices into the coronary or peripheral vascular systems.
Envoy - The Envoy guiding catheter is intended for use in the peripheral, coronary, and neurovasculature for the intravascular introduction of interventional / diagnostic devices.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K021593 · printed Nov 4, 2026
Cite this page
510(k) Report. “K021593: Modification to Envoy and Vista Brite Tip.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K021593
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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