510(k) · Cleared

Cleared

Scimed Avenue Coronary Guidewire Insertion Tool

K922410510(k) TraditionalCleared Jul 23, 199263-day reviewClass II21 CFR 870.1330

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

Scimed Life Systems, Inc. · DQX Wire, Guide, Catheter

Cleared on Jul 23, 1992 after a 63-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 3 later devices descend from it.

Decided: Jul 23, 1992
Review: 63 days
Class: Class II
Product code: DQX
Recalls: None
Predicates: 0

3 later devices descend from it, 2 citing it directly.

This deviceK922410 Scimed Avenue Coronary Guidewire Insertion ToolScimed Life Systems, Inc. · 1992
Descendant · cites it directly · 1 of its ownK140673 Insertion ToolBoston Scientific Corp · 2014
Descendant · 2 generations on · 0 of its ownK172453 WATCHDOG Hemostasis Valve KitBoston Scientific Corporation · 2017 · Recalled
Descendant · cites it directly · 0 of its ownK140745 Encore 26 Advantage KitBoston Scientific Corp · 2014 · Recalled

Most influential descendants

Showing 3 of 3 · See all

K140673Insertion ToolBoston Scientific Corp · 2014 · cites it directly1descendant
K172453WATCHDOG Hemostasis Valve KitBoston Scientific Corporation · 2017 · 2 generations on0descendants
K140745Encore 26 Advantage KitBoston Scientific Corp · 2014 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K922410	Scimed Avenue Coronary Guidewire Insertion Tool	Scimed Life Systems, Inc.	1992	—
+1	K140673	Insertion Tool	Boston Scientific Corp	2014	—
+2	K172453	WATCHDOG Hemostasis Valve Kit	Boston Scientific Corporation	2017	2
+1	K140745	Encore 26 Advantage Kit	Boston Scientific Corp	2014	1

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2014	2	0
2017	1	0

FIG. 1 — Lineage of K922410, 1992–2017Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DQX? 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 DQX device

#1 K213854 SavvyWirescore 15.7 · 10 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (3)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K140673	Insertion Tool	Boston Scientific Corp	2014	1
K140745	Encore 26 Advantage Kit	Boston Scientific Corp	2014	0

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?

Of its descendants, K140673 (Boston Scientific Corp, 2014) has gone furthest, with 1 descendant of its own.

How does its category compare?

All DQX devices

DQX Wire, Guide, Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DQX

10in 2025

2007high 21 (2010) · low 6 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DQX

177in 2025

2007high 212 (2022) · low 43 (2011)2026

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

Recalls per year · DQX

3in 2024

2007high 49 (2009) · low 0 (2014)2026

Class I (8 since 2007) Class II/III not classified

Adverse event reports per year · DQX

2,178in 2025

2007high 2,210 (2024) · low 687 (2009)2025

MAUDE reports naming product code DQX, 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	14	85	12	760
2008	19	87	7	715
2009	18	87	49	687
2010	21	63	34	987
2011	18	43	3	1,311
2012	20	62	5	1,337
2013	18	119	7 (4)	1,474
2014	18	103	0	1,323
2015	15	112	1	1,323
2016	14	179	2 (2)	1,466
2017	19	85	17	1,524
2018	19	114	9	1,737
2019	13	173	2	1,679
2020	14	106	1 (1)	1,536
2021	6	161	0	1,713
2022	15	212	0	1,647
2023	10	136	0	2,068
2024	11	134	3	2,210
2025	10	177	0	2,178
2026	12	145	4 (1)	—

https://510kreport.com/device/K922410 · printed Nov 6, 2026

Cite this page

510(k) Report. “K922410: Scimed Avenue Coronary Guidewire Insertion Tool.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K922410

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Record history

FDA decision record loaded May 2, 2026
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026