510(k) Report

510(k) · Cleared

Cleared

Asahi Guide Wire Extension, Model AG149000

K083145510(k) SpecialCleared Jan 12, 200981-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 Jan 12, 2009 as substantially equivalent to K022762 (Jomed, Inc., 2002) and 1 other predicate after an 81-day review. Its family tree reaches back 5 generations to 1989. 14 later devices descend from it.

Decided
Jan 12, 2009
Review
81 days
Class
Class II
Product code
DQX
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K890505 (1989). 16 ancestors in all. 14 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 1 other ancestor1998: 4 other ancestors1997: 1 other ancestor1995: 2 other ancestors1993: 1 other ancestor1994: 2 other ancestors2017: 1 descendant cleared2011: 1 descendant cleared2022: 2 descendants cleared2021: 2 descendants cleared2018: 1 descendant cleared2024: 1 descendant cleared2025: 3 descendants cleared2023: 3 descendants clearedK890505 · 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. · 1999K022762 · Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000, AG141002, AG141010, AG14M060 & AG14M050 · Jomed, Inc. · 2002K061984 · Treasure · Asahi Intecc Co., Ltd. · 20061990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 3 other ancestors3 generations back: 5 other ancestors4 generations back: 3 other ancestors 1 generation forward: 2 descendants2 generations forward: 8 descendants3 generations forward: 4 descendants K061984 · Treasure · Asahi Intecc Co., Ltd. · 2006K022762 · Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000, AG141002, AG141010, AG14M060 & AG14M050 · Jomed, Inc. · 2002K990639 · Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with Hydrocoat Hydrophilic Coating. · Guidant Corp. · 1999K961271 · Usci Commander Series Guide Wires · C.R. Bard, Inc. · 1996K890505 · Usci Grey/Black Guide Wire · C.R. Bard, Inc. · 1989−50
  1. Root · 5 generations backK890505 Usci Grey/Black Guide WireC.R. Bard, Inc. · 1989
  2. 4 generations backK961271 Usci Commander Series Guide WiresC.R. Bard, Inc. · 1996
  3. 3 generations backK990639 Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with…Guidant Corp. · 1999
  4. 2 generations backK022762 Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000…Jomed, Inc. · 2002
  5. 1 generation backK061984 TreasureAsahi Intecc Co., Ltd. · 2006
  6. This deviceK083145 Asahi Guide Wire Extension, Model AG149000Asahi Intecc Co., Ltd. · 2009
  7. Descendant · cites it directly · 13 of its ownK101985 Asahi Guide Wire Extension 165CMAsahi Intecc Co., Ltd. · 2011
  8. Descendant · cites it directly · 11 of its ownK163426 ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide…Asahi Intecc Co., Ltd. · 2017
  9. Descendant · 2 generations on · 3 of its ownK203533 Vassallo GTFilmecc Co., Ltd. · 2021
  10. Descendant · 2 generations on · 1 of its ownK203529 VASSALLO GT HybridFilmecc Co., Ltd. · 2021
  11. Descendant · 2 generations on · 0 of its ownK243733 SION blue PLUSAsahi Intecc Co., Ltd. · 2025

Showing 5 of 14 descendants. See all descendants

Descendants cleared per year

2011: 12017: 12018: 12021: 22022: 22023: 32024: 12025: 3
2011high 3 (2023) · low 0 (2012)2026

Most influential descendants

Showing 5 of 14 · See all
  • K101985Asahi Guide Wire Extension 165CMAsahi Intecc Co., Ltd. · 2011 · cites it directly13descendants
  • K163426ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire ExtensionAsahi Intecc Co., Ltd. · 2017 · cites it directly11descendants
  • K203533Vassallo GTFilmecc Co., Ltd. · 2021 · 2 generations on3descendants
  • K203529VASSALLO GT HybridFilmecc Co., Ltd. · 2021 · 2 generations on1descendant
  • K243733SION blue PLUSAsahi Intecc Co., Ltd. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K890505Usci Grey/Black Guide WireC.R. Bard, Inc.1989—
−4K961271Usci Commander Series Guide WiresC.R. Bard, Inc.1996—
−3K990639Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with Hydrocoat…Guidant Corp.1999—
−2K022762Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000…Jomed, Inc.2002—
−1K061984TreasureAsahi Intecc Co., Ltd.2006—
0 (this device)K083145Asahi Guide Wire Extension, Model AG149000Asahi Intecc Co., Ltd.2009—
+1K101985Asahi Guide Wire Extension 165CMAsahi Intecc Co., Ltd.2011—
+1K163426ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire…Asahi Intecc Co., Ltd.2017—
+2K203533Vassallo GTFilmecc Co., Ltd.2021—
+2K203529VASSALLO GT HybridFilmecc Co., Ltd.2021—
+2K243733SION blue PLUSAsahi Intecc Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199420
199520
199710
199840
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201710
201810
202120
202220
202330
202410
202530
FIG. 1 — Lineage of K083145, 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K022762Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000, AG141002…
Summary page 1
…re, Guide, Catheter DEVICE Class 2 per 21 CFR §870.1330 CLASSIFICATION: PRODUCT CODE DQX PREDICATE DEVICE: Asahi JoWire Neo's PTCA Guide Wire - K022762 Asahi Treasure 12 Peripheral Guide Wire - K061984 DESCRIPTION OF THE DEVICE SUBJECT TO PREMARKET NOTIFICATI…
Jomed, Inc.2002—
*K061984Treasure
Summary page 1
…330 CLASSIFICATION: PRODUCT CODE DQX PREDICATE DEVICE: Asahi JoWire Neo's PTCA Guide Wire - K022762 Asahi Treasure 12 Peripheral Guide Wire - K061984 DESCRIPTION OF THE DEVICE SUBJECT TO PREMARKET NOTIFICATION: The Asahi Guide Wire 'Extension accessory is used to elongate th…
Asahi Intecc Co., Ltd.2006—

Also cleared against K022762: 22 other devices →

What descends from it? (14)

See all 14

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

NumberDeviceApplicantDecidedDescendants
K101985Asahi Guide Wire Extension 165CMAsahi Intecc Co., Ltd.201113
K163426ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire ExtensionAsahi Intecc Co., Ltd.201711

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 20 years and passes through 4 companies; a new generation was cleared every 3.7 years on median.
  • 2 of the 16 ancestors have a recall of any class.
  • Of its descendants, K101985 (Asahi Intecc Co., Ltd., 2011) has gone furthest, with 13 descendants of its own.
  • 22 other devices also cite its predicate K022762.

How does its category compare?

All DQX devices

DQX Wire, Guide, Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, 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?

The Asahi Guide Wire Extension accessory is intended for extension of the working length of an already introduced guide wire when exchanging over-the-wire interventional devices during an angioplasty procedure.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K083145: Asahi Guide Wire Extension, Model AG149000.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K083145

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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