510(k) Report

510(k) · Cleared

Cleared

ASAHI Gladius Mongo18 PV ES

K213868510(k) TraditionalCleared Sep 6, 2022270-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

Asahi Intecc Co., Ltd. · DQX Wire, Guide, Catheter

Cleared on Sep 6, 2022 as substantially equivalent to K150445 (Asahi Intecc Co., Ltd., 2015) after a 270-day review. Its family tree reaches back 11 generations to 1989. 1 later device descends from it.

Decided
Sep 6, 2022
Review
270 days
Class
Class II
Product code
DQX
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K890505 (1989). 29 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2007: 2 other ancestors2006: 1 other ancestor2005: 2 other ancestors1998: 4 other ancestors2004: 2 other ancestors1997: 1 other ancestor1995: 2 other ancestors1994: 2 other ancestors1993: 1 other ancestor2025: 1 descendant clearedReference device: K072431 · Asahi Ptca Guide Wire, X-Treme · Asahi Intecc Co., Ltd. · 2007Reference device: K163426 · ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire Extension · Asahi Intecc Co., Ltd. · 2017Reference device: K180784 · ASAHI PTCA Guide Wire ASAHI Gladius Mongo 14, ASAHI Gladius Mongo 14 ES · Asahi Intecc Co., Ltd. · 2018K890505 · Usci Grey/Black Guide Wire · C.R. Bard, Inc. · 1989K961271 · Usci Commander Series Guide Wires · C.R. Bard, Inc. · 1996K990639 · Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with Hydrocoat Hydrophilic Coating. · Guidant Corp. · 1999×3: 3 generations cleared close together, K022762 (2002), K031277 (2003), K032615 (2003) K043422 · Asahi Ptca Guide Wire, J Shape Series · Asahi Intecc Co., Ltd. · 2005K062186 · Asahi Ptca Guide Wire, Fielder J, Model AGP140000J, AGP140300J · Asahi Intecc Co., Ltd. · 2006K070945 · Asahi Ptca Guide Wire · Asahi Intecc Co., Ltd. · 2008K103057 · Asahi Astato XS 20 Peripheral Guide Wire · Asahi Intecc Co., Ltd. · 2010K150445 · ASAHI Peripheral Guide Wire Series (ASAHI Gladius, ASAHI Halberd, ASAHI Gaia PV) · Asahi Intecc Co., Ltd. · 20151990200020102020
  1. Root · 11 generations backK890505 Usci Grey/Black Guide WireC.R. Bard, Inc. · 1989
  2. 7 generations between
  3. 3 generations backK070945 Asahi Ptca Guide WireAsahi Intecc Co., Ltd. · 2008
  4. 2 generations backK103057 Asahi Astato XS 20 Peripheral Guide WireAsahi Intecc Co., Ltd. · 2010
  5. 1 generation backK150445 ASAHI Peripheral Guide Wire Series (ASAHI Gladius, ASAHI Halberd…Asahi Intecc Co., Ltd. · 2015
  6. This deviceK213868 ASAHI Gladius Mongo18 PV ESAsahi Intecc Co., Ltd. · 2022
  7. Descendant · cites it directly · 0 of its ownK242597 CROSSLEAD 0.018inchAsahi Intecc Co., Ltd. · 2025
Show all 11 generations
  1. Root · 11 generations backK890505 Usci Grey/Black Guide WireC.R. Bard, Inc. · 1989
  2. 10 generations backK961271 Usci Commander Series Guide WiresC.R. Bard, Inc. · 1996
  3. 9 generations backK990639 Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with…Guidant Corp. · 1999
  4. 8 generations backK022762 Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000…Jomed, Inc. · 2002
  5. 7 generations backK031277 Jowire Asahi Ptca Catheter Guide Wires, Models…Jomed, Inc. · 2003
  6. 6 generations backK032615 Asahi Ptca Catheter Guide Wires, Models AGH147000 and AGH147300Asahi Intecc Co., Ltd. · 2003
  7. 5 generations backK043422 Asahi Ptca Guide Wire, J Shape SeriesAsahi Intecc Co., Ltd. · 2005
  8. 4 generations backK062186 Asahi Ptca Guide Wire, Fielder J, Model AGP140000J, AGP140300JAsahi Intecc Co., Ltd. · 2006
  9. 3 generations backK070945 Asahi Ptca Guide WireAsahi Intecc Co., Ltd. · 2008
  10. 2 generations backK103057 Asahi Astato XS 20 Peripheral Guide WireAsahi Intecc Co., Ltd. · 2010
  11. 1 generation backK150445 ASAHI Peripheral Guide Wire Series (ASAHI Gladius, ASAHI Halberd…Asahi Intecc Co., Ltd. · 2015
  12. This deviceK213868 ASAHI Gladius Mongo18 PV ESAsahi Intecc Co., Ltd. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K242597CROSSLEAD 0.018inchAsahi Intecc Co., Ltd. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K890505Usci Grey/Black Guide WireC.R. Bard, Inc.1989—
−10K961271Usci Commander Series Guide WiresC.R. Bard, Inc.1996—
−9K990639Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with Hydrocoat…Guidant Corp.1999—
−8K022762Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000…Jomed, Inc.2002—
−7K031277Jowire Asahi Ptca Catheter Guide Wires, Models…Jomed, Inc.2003—
−6K032615Asahi Ptca Catheter Guide Wires, Models AGH147000 and AGH147300Asahi Intecc Co., Ltd.2003—
−5K043422Asahi Ptca Guide Wire, J Shape SeriesAsahi Intecc Co., Ltd.2005—
−4K062186Asahi Ptca Guide Wire, Fielder J, Model AGP140000J, AGP140300JAsahi Intecc Co., Ltd.2006—
−3K070945Asahi Ptca Guide WireAsahi Intecc Co., Ltd.2008—
−2K103057Asahi Astato XS 20 Peripheral Guide WireAsahi Intecc Co., Ltd.2010—
−1K150445ASAHI Peripheral Guide Wire Series (ASAHI Gladius, ASAHI Halberd, ASAHI Gaia PV)Asahi Intecc Co., Ltd.2015—
0 (this device)K213868ASAHI Gladius Mongo18 PV ESAsahi Intecc Co., Ltd.2022—
+1K242597CROSSLEAD 0.018inchAsahi Intecc Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199420
199520
199710
199840
200420
200520
200610
200720
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K213868, 1989–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

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 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K150445ASAHI Peripheral Guide Wire Series (ASAHI Gladius, ASAHI Halberd, ASAHI Gaia PV)
Summary page 5
…SSIFICATION NAME: Catheter Guide Wire PRODUCT CODE: DQX PREDICATE DEVICE(S): ASAHI Peripheral Guide Wires (K150445) REFERENCE DEVICE(S): ASAHI PTCA Guide Wire FIELDER XT (K072431) A…
Asahi Intecc Co., Ltd.2015—
†K072431Asahi Ptca Guide Wire, X-TremeAsahi Intecc Co., Ltd.2007—
†K163426ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire ExtensionAsahi Intecc Co., Ltd.2017—
†K180784ASAHI PTCA Guide Wire ASAHI Gladius Mongo 14, ASAHI Gladius Mongo 14 ESAsahi Intecc Co., Ltd.2018—

Also cleared against K150445: 5 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K242597CROSSLEAD 0.018inchAsahi Intecc Co., Ltd.20250

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 33 years and passes through 4 companies; a new generation was cleared every 2.7 years on median.
  • 2 of the 29 ancestors have a recall of any class.
  • Of its descendants, K242597 (Asahi Intecc Co., Ltd., 2025) has gone furthest, with 0 descendants of its own.
  • 5 other devices also cite its predicate K150445.

How does its category compare?

All DQX devices

DQX Wire, Guide, Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

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)—

What is it indicated for?

This product is intended to facilitate the placement and exchange of diagnostic and therapeutic devices during intravascular procedures. This device is intended for peripheral vascular use only.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K213868: ASAHI Gladius Mongo18 PV ES.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K213868

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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