510(k) Report

510(k) · Cleared

Cleared

Asahi Ptca Guide Wire, Fielder FC J, Models: AGP140001J, AGP140301J

K072705510(k) SpecialCleared Oct 23, 200729-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 Oct 23, 2007 as substantially equivalent to K052022 (Asahi Intecc Co., Ltd., 2005) and 1 other predicate after a 29-day review. Its family tree reaches back 7 generations to 1989. 22 later devices descend from it.

Decided
Oct 23, 2007
Review
29 days
Class
Class II
Product code
DQX
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K890505 (1989). 10 ancestors in all. 22 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1998: 3 other ancestors2017: 1 descendant cleared2016: 1 descendant cleared2018: 4 descendants cleared2021: 3 descendants cleared2024: 1 descendant cleared2025: 3 descendants cleared2022: 4 descendants cleared2020: 2 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. · 1999×2: 2 generations cleared close together, K022762 (2002), K031277 (2003) K052022 · Asahi Ptca Guide Wire Fielder · Asahi Intecc Co., Ltd. · 2005K063819 · Asahi Ptca Guide Wire, Fielder FC · Asahi Intecc Co., Ltd. · 20071990200020102020
  1. Root · 7 generations backK890505 Usci Grey/Black Guide WireC.R. Bard, Inc. · 1989
  2. 6 generations backK961271 Usci Commander Series Guide WiresC.R. Bard, Inc. · 1996
  3. 5 generations backK990639 Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with…Guidant Corp. · 1999
  4. 4 generations backK022762 Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000…Jomed, Inc. · 2002
  5. 3 generations backK031277 Jowire Asahi Ptca Catheter Guide Wires, Models…Jomed, Inc. · 2003
  6. 2 generations backK052022 Asahi Ptca Guide Wire FielderAsahi Intecc Co., Ltd. · 2005
  7. 1 generation backK063819 Asahi Ptca Guide Wire, Fielder FCAsahi Intecc Co., Ltd. · 2007
  8. This deviceK072705 Asahi Ptca Guide Wire, Fielder FC J, Models: AGP140001J, AGP140301JAsahi Intecc Co., Ltd. · 2007
  9. Descendant · cites it directly · 21 of its ownK153106 ASAHI Fielder XT-A, ASAHI Fielder XT-RAsahi Intecc Co., Ltd. · 2016
  10. Descendant · cites it directly · 11 of its ownK163426 ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide…Asahi Intecc Co., Ltd. · 2017
  11. Descendant · 2 generations on · 7 of its ownK171933 ASAHI PTCA Guide Wires, ASAHI Corsair Microcatheter, ASAHI Corsair…Asahi Intecc Co., Ltd. · 2018
  12. Descendant · 2 generations on · 3 of its ownK203533 Vassallo GTFilmecc Co., Ltd. · 2021
  13. Descendant · 3 generations on · 1 of its ownK212211 Turnpike catheter, Turnpike Spiral catheter, Turnpike LP catheter…Vascular Solutions, LLC · 2022

Showing 5 of 22 descendants. See all descendants

Descendants cleared per year

2016: 12017: 12018: 42020: 22021: 32022: 42023: 32024: 12025: 3
2016high 4 (2018) · low 0 (2019)2026

Most influential descendants

Showing 5 of 22 · See all
  • K153106ASAHI Fielder XT-A, ASAHI Fielder XT-RAsahi Intecc Co., Ltd. · 2016 · cites it directly21descendants
  • K163426ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire ExtensionAsahi Intecc Co., Ltd. · 2017 · cites it directly11descendants
  • K171933ASAHI PTCA Guide Wires, ASAHI Corsair Microcatheter, ASAHI Corsair Pro MicrocatheterAsahi Intecc Co., Ltd. · 2018 · 2 generations on7descendants
  • K203533Vassallo GTFilmecc Co., Ltd. · 2021 · 2 generations on3descendants
  • K212211Turnpike catheter, Turnpike Spiral catheter, Turnpike LP catheter, Turnpike Gold…Vascular Solutions, LLC · 2022 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K890505Usci Grey/Black Guide WireC.R. Bard, Inc.1989—
−6K961271Usci Commander Series Guide WiresC.R. Bard, Inc.1996—
−5K990639Acs HI-Torque Cross IT 100XT, 200XT and 300XT Guide Wires with Hydrocoat…Guidant Corp.1999—
−4K022762Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000…Jomed, Inc.2002—
−3K031277Jowire Asahi Ptca Catheter Guide Wires, Models…Jomed, Inc.2003—
−2K052022Asahi Ptca Guide Wire FielderAsahi Intecc Co., Ltd.2005—
−1K063819Asahi Ptca Guide Wire, Fielder FCAsahi Intecc Co., Ltd.2007—
0 (this device)K072705Asahi Ptca Guide Wire, Fielder FC J, Models: AGP140001J, AGP140301JAsahi Intecc Co., Ltd.2007—
+1K153106ASAHI Fielder XT-A, ASAHI Fielder XT-RAsahi Intecc Co., Ltd.2016—
+1K163426ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire…Asahi Intecc Co., Ltd.2017—
+2K171933ASAHI PTCA Guide Wires, ASAHI Corsair Microcatheter, ASAHI Corsair Pro…Asahi Intecc Co., Ltd.2018—
+2K203533Vassallo GTFilmecc Co., Ltd.2021—
+3K212211Turnpike catheter, Turnpike Spiral catheter, Turnpike LP catheter, Turnpike…Vascular Solutions, LLC2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199830

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201710
201840
202020
202130
202240
202330
202410
202530
FIG. 1 — Lineage of K072705, 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
*K052022Asahi Ptca Guide Wire Fielder
Summary page 1
…Catheter Guide Wire DEVICE Class 2 per 21 CFR §870.1330 CLASSIFICATION: PRODUCT CODE DQX PRIMARY Asahi PTCA Guide Wire, Fielder - K052022 PREDICATE DEVICE: Asahi PTCA Guide Wire, Fielder FC- K063819 DESCRIPTION OF THE DEVICE SUBJECT TO PREMARKET NOTIFICATION: The…
Asahi Intecc Co., Ltd.2005—
*K063819Asahi Ptca Guide Wire, Fielder FC
Summary page 1
…1 CFR §870.1330 CLASSIFICATION: PRODUCT CODE DQX PRIMARY Asahi PTCA Guide Wire, Fielder - K052022 PREDICATE DEVICE: Asahi PTCA Guide Wire, Fielder FC- K063819 DESCRIPTION OF THE DEVICE SUBJECT TO PREMARKET NOTIFICATION: The Asahi PTCA Guide Wire, Fielder FC J is a steerable guide wir…
Asahi Intecc Co., Ltd.2007—

Also cleared against K052022: 7 other devices →

What descends from it? (22)

See all 22

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

NumberDeviceApplicantDecidedDescendants
K153106ASAHI Fielder XT-A, ASAHI Fielder XT-RAsahi Intecc Co., Ltd.201621
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 18 years and passes through 4 companies; a new generation was cleared every 2.3 years on median.
  • None of the 10 ancestors has a recall.
  • Of its descendants, K153106 (Asahi Intecc Co., Ltd., 2016) has gone furthest, with 21 descendants of its own.
  • 7 other devices also cite its predicate K052022.

How does its category compare?

All DQX devices

DQX Wire, Guide, Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, 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 PTCA Guide Wire, Fielder FC J is intended to facilitate the placement of

balloon dilatation catheters during percutaneous transluminal coronary angioplasty

(PTCA) and percutaneous transluminal angioplasty (PTA). The Asahi PTCA Guide

Wires are not to be used in the cerebral blood vessel.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K072705: Asahi Ptca Guide Wire, Fielder FC J, Models: AGP140001J, AGP140301J.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K072705

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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