510(k) · Cleared

Cleared

HI-Torque Pilot 50 Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque Pilot 150 Guide Wire with Hydrocoat Hydrophg

K030549510(k) SpecialCleared May 14, 200382-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

Guidcorp · DQX Wire, Guide, Catheter

Cleared on May 14, 2003 as substantially equivalent to K002206 (Guidant Corp., 2000) and 2 other predicates after an 82-day review. Its family tree reaches back 3 generations to 2000. 1 of the 22 devices in its family, counting itself, has a Class I recall. 18 later devices descend from it.

Decided: May 14, 2003
Review: 82 days
Class: Class II
Product code: DQX
Recalls: None
Predicates: 3

Its longest line of descent runs back 3 generations to K002206 (2000). 18 later devices descend from it, 3 citing it directly. 1 of the 22 devices in this family, counting this one, has a Class I recall.

By dateBy generation

Root · 3 generations backK002206 HI-Torque Whisper LS Guide Wire with Hydrocoat Hydrophilic Coating…Guidant Corp. · 2000
2 generations backK013092 HI-Toque Whisper LS and MS Guide Wire with Hydrocoat Hydrophilic…Guidant Corp. · 2001
1 generation backK020340 Modification to HI-Torque Whisper LS and MS Guide Wires with…Guidant Corp. · 2002
This deviceK030549 HI-Torque Pilot 50 Guide Wire with Hydrocoat Hydrophilic Coating…Guidcorp · 2003
Descendant · cites it directly · 10 of its ownK101116 HI-Torque Pilot 50 and 150 Guide Wire with Hydrocoat Hydrophilic…Abbott Vascular-Cardiac Therapies · 2010
Descendant · cites it directly · 9 of its ownK091825 HI-Torque Progress Guide Wire FamilyAbbott Vascular, Inc. · 2009
Descendant · 2 generations on · 6 of its ownK122573 HI-Torque Command Guide Wire FamilyAbbott Vascular, Inc. · 2012
Descendant · 2 generations on · 4 of its ownK101011 HI-Torque Balance Middleweight UniversalAbbott Vascular, Inc. · 2010
Descendant · 3 generations on · 2 of its ownK152709 HI-Torque BalanceAbbott Vascular · 2015

Showing 5 of 18 descendants. See all descendants

Descendants cleared per year

2009high 3 (2010) · low 0 (2011)2026

Class I recalls in this family

K121398 Charlie Guidewire (Regular), Charlie Guidewire…3 generations on · 2012

Most influential descendants

Showing 5 of 18 · See all

K101116HI-Torque Pilot 50 and 150 Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque…Abbott Vascular-Cardiac Therapies · 2010 · cites it directly10descendants
K091825HI-Torque Progress Guide Wire FamilyAbbott Vascular, Inc. · 2009 · cites it directly9descendants
K122573HI-Torque Command Guide Wire FamilyAbbott Vascular, Inc. · 2012 · 2 generations on6descendants
K101011HI-Torque Balance Middleweight UniversalAbbott Vascular, Inc. · 2010 · 2 generations on4descendants
K152709HI-Torque BalanceAbbott Vascular · 2015 · 3 generations on2descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−3	K002206	HI-Torque Whisper LS Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque…	Guidant Corp.	2000	—
−2	K013092	HI-Toque Whisper LS and MS Guide Wire with Hydrocoat Hydrophilic Coating	Guidant Corp.	2001	—
−1	K020340	Modification to HI-Torque Whisper LS and MS Guide Wires with Hydrocoat…	Guidant Corp.	2002	—
0 (this device)	K030549	HI-Torque Pilot 50 Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque…	Guidcorp	2003	—
+1	K101116	HI-Torque Pilot 50 and 150 Guide Wire with Hydrocoat Hydrophilic Coating…	Abbott Vascular-Cardiac Therapies	2010	—
+1	K091825	HI-Torque Progress Guide Wire Family	Abbott Vascular, Inc.	2009	—
+2	K122573	HI-Torque Command Guide Wire Family	Abbott Vascular, Inc.	2012	—
+2	K101011	HI-Torque Balance Middleweight Universal	Abbott Vascular, Inc.	2010	—
+3	K152709	HI-Torque Balance	Abbott Vascular	2015	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2009	1	0
2010	3	0
2012	2	1
2013	1	0
2014	1	0
2015	2	0
2017	2	0
2019	3	0
2020	1	0
2024	1	0
2025	1	0

FIG. 1 — Lineage of K030549, 2000–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 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? (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	Applicant	Decided	Recalls
*	K002206	HI-Torque Whisper LS Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque Whisper MS… Summary page 1 …ivalent with regard to these features in the predicate device, the HI-TORQUE WHISPERTMMS Guide Wire with Hydrocoat Hydrophilic Coating (K002206, August 24,2000; K013092, December 13,2001; and K020340, March 1, 2002).…	Guidant Corp.	2000	—
*	K013092	HI-Toque Whisper LS and MS Guide Wire with Hydrocoat Hydrophilic Coating Summary page 1 …ese features in the predicate device, the HI-TORQUE WHISPERTMMS Guide Wire with Hydrocoat Hydrophilic Coating (K002206, August 24,2000; K013092, December 13,2001; and K020340, March 1, 2002).…	Guidant Corp.	2001	—
*	K020340	Modification to HI-Torque Whisper LS and MS Guide Wires with Hydrocoat Hydrophilic Coating Summary page 1 …the HI-TORQUE WHISPERTMMS Guide Wire with Hydrocoat Hydrophilic Coating (K002206, August 24,2000; K013092, December 13,2001; and K020340, March 1, 2002). 17 Dev…	Guidant Corp.	2002	—

Also cleared against K002206: 3 other devices →

What descends from it? (18)

See all 18

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

Number	Device	Applicant	Decided	Descendants
K101116	HI-Torque Pilot 50 and 150 Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque…	Abbott Vascular-Cardiac Therapies	2010	10
K091825	HI-Torque Progress Guide Wire Family	Abbott Vascular, Inc.	2009	9
K123067	Progress Guide Wire Family, Pilot Guide Wire Family	Abbott Vascular, Inc.	2013	2

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.

K121398Charlie Guidewire (Regular), Charlie Guidewire (Stiff)Guidepath Medical, Inc. · 2012 · 3 generations on · ◆ in the 2012 descendants bar of FIG. 112 Class I recalls

What does this lineage say?

The line of descent spans 3 years and passes through 2 companies; a new generation was cleared every 1.2 years on median.
None of the 3 ancestors has a recall.
Of its descendants, K101116 (Abbott Vascular-Cardiac Therapies, 2010) has gone furthest, with 10 descendants of its own.
3 other devices also cite its predicate K002206.

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)	—

What is it indicated for?

To facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA) and compatible stent devices.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K030549 · printed Nov 6, 2026

Cite this page

510(k) Report. “K030549: HI-Torque Pilot 50 Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque Pilot 150 Guide Wire with Hydrocoat Hydrophg.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K030549

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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