510(k) Report

510(k) · Cleared

Cleared

0.016 Guide Wire for Neurological Endoscope

K913074510(k) TraditionalCleared Nov 5, 1991117-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

Terumo Medical Corp. · DQX Wire, Guide, Catheter

Cleared on Nov 5, 1991 after a 117-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 11 later devices descend from it.

Decided
Nov 5, 1991
Review
117 days
Class
Class II
Product code
DQX
Recalls
None
Predicates
0

11 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2005: 1 descendant cleared2006: 1 descendant cleared2019: 1 descendant cleared2023: 1 descendant cleared2020: 1 descendant cleared2025: 2 descendants cleared2026: 4 descendants cleared1990200020102020
  1. This deviceK913074 0.016 Guide Wire for Neurological EndoscopeTerumo Medical Corp. · 1991
  2. Descendant · cites it directly · 10 of its ownK050964 PV 1900 Synchro 0.016 GuidewireBoston Scientific - Precision Vascular · 2005 · Recalled
  3. Descendant · 2 generations on · 9 of its ownK053268 PVS 2000 SYNCHRO2 GuidewireBoston Scientific - Precision Vascular · 2006 · Recalled
  4. Descendant · 3 generations on · 6 of its ownK202522 Synchro SELECT GuidewireStryker Neurovascular · 2020 · Recalled
  5. Descendant · 4 generations on · 4 of its ownK243756 0.014” Willow GuidewireArbor Endovascular, LLC · 2025
  6. Descendant · 5 generations on · 3 of its ownK253168 0.014” Willow GuidewireArbor Endovascular, LLC · 2025

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2005: 12006: 12019: 12020: 12023: 12025: 22026: 4
2005high 4 (2026) · low 0 (2007)2026

Most influential descendants

Showing 5 of 11 · See all
  • K050964PV 1900 Synchro 0.016 GuidewireBoston Scientific - Precision Vascular · 2005 · cites it directly10descendants
  • K053268PVS 2000 SYNCHRO2 GuidewireBoston Scientific - Precision Vascular · 2006 · 2 generations on9descendants
  • K202522Synchro SELECT GuidewireStryker Neurovascular · 2020 · 3 generations on6descendants
  • K2437560.014” Willow GuidewireArbor Endovascular, LLC · 2025 · 4 generations on4descendants
  • K2531680.014” Willow GuidewireArbor Endovascular, LLC · 2025 · 5 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K9130740.016 Guide Wire for Neurological EndoscopeTerumo Medical Corp.1991—
+1K050964PV 1900 Synchro 0.016 GuidewireBoston Scientific - Precision Vascular20056
+2K053268PVS 2000 SYNCHRO2 GuidewireBoston Scientific - Precision Vascular200613
+3K202522Synchro SELECT GuidewireStryker Neurovascular20201
+4K2437560.014” Willow GuidewireArbor Endovascular, LLC2025—
+5K2531680.014” Willow GuidewireArbor Endovascular, LLC2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
200610
201910
202010
202310
202520
202640
FIG. 1 — Lineage of K913074, 1991–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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

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. #1 K213854 SavvyWirescore 15.7 · 10 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

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
K050964PV 1900 Synchro 0.016 GuidewireBoston Scientific - Precision Vascular200510

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, K050964 (Boston Scientific - Precision Vascular, 2005) has gone furthest, with 10 descendants 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

2007: 142008: 192009: 182010: 212011: 182012: 202013: 182014: 182015: 152016: 142017: 192018: 192019: 132020: 142021: 62022: 152023: 102024: 112025: 102026 (partial year): 12
2007high 21 (2010) · low 6 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DQX

177in 2025

2007: 85 days median2008: 87 days median2009: 87 days median2010: 63 days median2011: 43 days median2012: 62 days median2013: 119 days median2014: 103 days median2015: 112 days median2016: 179 days median2017: 85 days median2018: 114 days median2019: 173 days median2020: 106 days median2021: 161 days median2022: 212 days median2023: 136 days median2024: 134 days median2025: 177 days median2026 (partial year): 145 days median
2007high 212 (2022) · low 43 (2011)2026

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

Recalls per year · DQX

3in 2024

2007: 122008: 72009: 492010: 342011: 32012: 52013: 7, 4 Class I2015: 12016: 2, 2 Class I2017: 172018: 92019: 22020: 1, 1 Class I2024: 32026 (partial year): 4, 1 Class I
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

2007: 7602008: 7152009: 6872010: 9872011: 1,3112012: 1,3372013: 1,4742014: 1,3232015: 1,3232016: 1,4662017: 1,5242018: 1,7372019: 1,6792020: 1,5362021: 1,7132022: 1,6472023: 2,0682024: 2,2102025: 2,178
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007148512760
200819877715
2009188749687
2010216334987
2011184331,311
2012206251,337
2013181197 (4)1,474
20141810301,323
20151511211,323
2016141792 (2)1,466
20171985171,524
20181911491,737
20191317321,679
2020141061 (1)1,536
2021616101,713
20221521201,647
20231013602,068
20241113432,210
20251017702,178
2026121454 (1)—

More from Terumo Medical Corp.

143 FDA decisions under this applicant name. See the company

  • K111606Pinnacle Precision Access SystemTerumo Medical Corp. · 20111 recall
  • K111556Glidecross Support CatheterTerumo Medical Corp. · 2011
  • K110540Terumo Support CatheterTerumo Medical Corp. · 2011
  • K102008GlidesheathTerumo Medical Corp. · 20101 recall
  • K091329Pinnacle Destination Peripheral Guiding SheathTerumo Medical Corp. · 20091 recall

Recent decisions in DQX

The DQX category page

  • K260168Small Diameter Core Wire (CMAN-000-00); Small Diameter Core Wire (CMAN-000-14)Skycade Med Corporation · 2026
  • K253146Hyperdrive 35 GuidewireRapid-Medical, Ltd. · 2026
  • K261281CROSSLEAD Standard 035 and CROSSLEAD Stiff 035Filmecc Co., Ltd. · 2026
  • K253667Accoat Guide WireSp Medical A/S · 2026
  • K261640Merit MAK Nitinol/Gold-Tungsten Guide WireMerit Medical Ireland, Ltd. · 2026

https://510kreport.com/device/K913074 · printed Nov 6, 2026

Cite this page

510(k) Report. “K913074: 0.016 Guide Wire for Neurological Endoscope.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K913074

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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