510(k) Report

510(k) · Cleared

Cleared

Arrow Jugular Axillo-Subclavian Central Catheter (Jacc)

K121501510(k) TraditionalCleared Nov 29, 2012192-day reviewClass II21 CFR 880.5970

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Arrow International (Subsidiary of Teleflex Inc.) · LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

Cleared on Nov 29, 2012 as substantially equivalent to K112896 (Arrow International (Subsidiary of Teleflex Inc.), 2012) and 1 other predicate after a 192-day review. Its family tree reaches back 10 generations to 2000. 7 of the 38 devices in its family, counting itself, have a Class I recall. 4 later devices descend from it.

Decided
Nov 29, 2012
Review
192 days
Class
Class II
Product code
LJS
Recalls
None
Predicates
2

Its longest line of descent runs back 10 generations to K001901 (2000). 33 ancestors in all, the oldest K830256 (1983). 4 later devices descend from it, 1 citing it directly. 7 of the 38 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor, 1 with a Class I recall12009: 1 other ancestor2006: 3 other ancestors2000: 2 other ancestors, 1 with a Class I recall11997: 1 other ancestor1990: 1 other ancestor, 1 with a Class I recall11989: 1 other ancestor1986: 1 other ancestor, 1 with a Class I recall12008: 1 other ancestor2005: 3 other ancestors2004: 2 other ancestors2003: 1 other ancestor1983: 1 other ancestor2001: 2 other ancestors1999: 1 other ancestor1996: 1 other ancestor2013: 1 descendant cleared, 1 with a Class I recall12015: 1 descendant cleared2016: 2 descendants cleared, 1 with a Class I recall1K001901 · Poly Per-Q-Cath Picc Catheter,Model 3236100 and Poly Per-Q-Cath Midline Catheter, Model 3134135 · C.R. Bard, Inc. · 2000 · recalledK012902 · Poly Per-Q-Cath Single Lumen Picc Catheter, Model 3143100; Poly Per-Q-Cath Dual Lumen Picc Catheter, Model 3246100 · C.R. Bard, Inc. · 2001K031129 · Poly Per-Q-Cath Picc Catheters; Poly Radpicc · C.R. Bard, Inc. · 2003K033389 · Powerpicc Catheters, Models 3175155, 3175135 · C.R. Bard, Inc. · 2004 · recalled×3: 3 generations cleared close together, K050185 (2005), K051417 (2005), K051991 (2005) K080604 · Pressure Injfectable Picc · Arrow International, Inc. · 2008 · recalledK100635 · Arrowgard Evolution Antimicrobial Peripherally Inserted Central Catheter (Picc) Model: S-44041-002, S-45041-002, S-45504 · Arrow Intl., Inc. · 2010K112896 · Arrw Evolution · Arrow International (Subsidiary of Teleflex Inc.) · 2012 · Class I recall19801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor, 1 with a Class I recall12 generations back: 7 other ancestors, 3 with a Class I recall33 generations back: 1 other ancestor4 generations back: 8 other ancestors5 generations back: 6 other ancestors 1 generation forward: 1 descendant, 1 with a Class I recall12 generations forward: 2 descendants, 1 with a Class I recall13 generations forward: 1 descendant K112896 · Arrw Evolution · Arrow International (Subsidiary of Teleflex Inc.) · 2012 · Class I recallK100635 · Arrowgard Evolution Antimicrobial Peripherally Inserted Central Catheter (Picc) Model: S-44041-002, S-45041-002, S-45504 · Arrow Intl., Inc. · 2010K080604 · Pressure Injfectable Picc · Arrow International, Inc. · 2008 · recalledK051991 · Powerpicc, Poly Per-Q-Cath, 6 FR TL Poly Per-Q-Cath, Power Hohn and Power Line · C.R. Bard, Inc. · 2005K051417 · 6 FR FL Powerhohn and Powerline Catheter · C.R. Bard, Inc. · 2005 · recalledK050185 · Powerhohn and Powerline Catheters · C.R. Bard, Inc. · 2005K033389 · Powerpicc Catheters, Models 3175155, 3175135 · C.R. Bard, Inc. · 2004 · recalledK031129 · Poly Per-Q-Cath Picc Catheters; Poly Radpicc · C.R. Bard, Inc. · 2003K012902 · Poly Per-Q-Cath Single Lumen Picc Catheter, Model 3143100; Poly Per-Q-Cath Dual Lumen Picc Catheter, Model 3246100 · C.R. Bard, Inc. · 2001K001901 · Poly Per-Q-Cath Picc Catheter,Model 3236100 and Poly Per-Q-Cath Midline Catheter, Model 3134135 · C.R. Bard, Inc. · 2000 · recalled−10−50
  1. Root · 10 generations backK001901 Poly Per-Q-Cath Picc Catheter,Model 3236100 and Poly Per-Q-Cath…C.R. Bard, Inc. · 2000 · Recalled
  2. 6 generations between
  3. 3 generations backK080604 Pressure Injfectable PiccArrow International, Inc. · 2008 · Recalled
  4. 2 generations backK100635 Arrowgard Evolution Antimicrobial Peripherally Inserted Central…Arrow Intl., Inc. · 2010
  5. 1 generation backK112896 Arrw EvolutionArrow International (Subsidiary of Teleflex Inc.) · 2012 · Recalled (Class I)
  6. This deviceK121501 Arrow Jugular Axillo-Subclavian Central Catheter (Jacc)Arrow International (Subsidiary of Teleflex Inc.) · 2012
  7. Descendant · cites it directly · 3 of its ownK132133 CG+ Arrow Jacc Powered by Arrow VPS StyletArrow International (Subsidiary of Teleflex Inc.) · 2013 · Recalled (Class I)
  8. Descendant · 2 generations on · 1 of its ownK153423 CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex, Inc.) · 2016 · Recalled (Class I)
  9. Descendant · 3 generations on · 0 of its ownK161765 CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex · 2016
  10. Descendant · 2 generations on · 0 of its ownK150109 Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter…Arrow International (A Subsidiary of Teleflex, Inc.) · 2015
Show all 10 generations
  1. Root · 10 generations backK001901 Poly Per-Q-Cath Picc Catheter,Model 3236100 and Poly Per-Q-Cath…C.R. Bard, Inc. · 2000 · Recalled
  2. 9 generations backK012902 Poly Per-Q-Cath Single Lumen Picc Catheter, Model 3143100; Poly…C.R. Bard, Inc. · 2001
  3. 8 generations backK031129 Poly Per-Q-Cath Picc Catheters; Poly RadpiccC.R. Bard, Inc. · 2003
  4. 7 generations backK033389 Powerpicc Catheters, Models 3175155, 3175135C.R. Bard, Inc. · 2004 · Recalled
  5. 6 generations backK050185 Powerhohn and Powerline CathetersC.R. Bard, Inc. · 2005
  6. 5 generations backK051417 6 FR FL Powerhohn and Powerline CatheterC.R. Bard, Inc. · 2005 · Recalled
  7. 4 generations backK051991 Powerpicc, Poly Per-Q-Cath, 6 FR TL Poly Per-Q-Cath, Power Hohn and…C.R. Bard, Inc. · 2005
  8. 3 generations backK080604 Pressure Injfectable PiccArrow International, Inc. · 2008 · Recalled
  9. 2 generations backK100635 Arrowgard Evolution Antimicrobial Peripherally Inserted Central…Arrow Intl., Inc. · 2010
  10. 1 generation backK112896 Arrw EvolutionArrow International (Subsidiary of Teleflex Inc.) · 2012 · Recalled (Class I)
  11. This deviceK121501 Arrow Jugular Axillo-Subclavian Central Catheter (Jacc)Arrow International (Subsidiary of Teleflex Inc.) · 2012

Class I recalls in this family

Most influential descendants

Showing 4 of 4 · See all
  • K132133CG+ Arrow Jacc Powered by Arrow VPS StyletArrow International (Subsidiary of Teleflex Inc.) · 2013 · cites it directly3descendants
  • K153423CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex, Inc.) · 2016 · 2 generations on1descendant
  • K161765CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex · 2016 · 3 generations on0descendants
  • K150109Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter (JACC) with Sustain…Arrow International (A Subsidiary of Teleflex, Inc.) · 2015 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K001901Poly Per-Q-Cath Picc Catheter,Model 3236100 and Poly Per-Q-Cath Midline…C.R. Bard, Inc.20002
−9K012902Poly Per-Q-Cath Single Lumen Picc Catheter, Model 3143100; Poly Per-Q-Cath…C.R. Bard, Inc.2001—
−8K031129Poly Per-Q-Cath Picc Catheters; Poly RadpiccC.R. Bard, Inc.2003—
−7K033389Powerpicc Catheters, Models 3175155, 3175135C.R. Bard, Inc.20041
−6K050185Powerhohn and Powerline CathetersC.R. Bard, Inc.2005—
−5K0514176 FR FL Powerhohn and Powerline CatheterC.R. Bard, Inc.20051
−4K051991Powerpicc, Poly Per-Q-Cath, 6 FR TL Poly Per-Q-Cath, Power Hohn and Power LineC.R. Bard, Inc.2005—
−3K080604Pressure Injfectable PiccArrow International, Inc.20081
−2K100635Arrowgard Evolution Antimicrobial Peripherally Inserted Central Catheter…Arrow Intl., Inc.2010—
−1K112896Arrw EvolutionArrow International (Subsidiary of Teleflex Inc.)2012Class I
0 (this device)K121501Arrow Jugular Axillo-Subclavian Central Catheter (Jacc)Arrow International (Subsidiary of Teleflex Inc.)2012—
+1K132133CG+ Arrow Jacc Powered by Arrow VPS StyletArrow International (Subsidiary of Teleflex Inc.)2013Class I
+2K153423CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex, Inc.)2016Class I
+3K161765CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex2016—
+2K150109Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter (JACC)…Arrow International (A Subsidiary of Teleflex, Inc.)2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198310
198611
198910
199011
199610
199710
199910
200021
200120
200310
200420
200530
200630
200711
200810
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201311
201510
201621
FIG. 1 — Lineage of K121501, 2000–2016Source: 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.

7 devices in this family have 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 LJS device

  1. #1 K241910 Neonav ECG Tip Location Systemscore 18.0 · 12 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
*K112896Arrw Evolution
Summary page 1
…r 3. Predicate Devices Predicate 1: ArrowEvolutionTM Pressure Injectable P1CC with Chlorag'ard Antimicrobial and Antithrombogenic Technology (K 112896) Predicate 2: Arrow Pressure Injectable CVC (K071538) 4. Device Descriition The Arrow Pressure Injectable Jugular Axil…
Arrow International (Subsidiary of Teleflex Inc.)2012Class I
*K071538Arrow, Arrowg+Ard and Arrowg+Ard Blue Plus Pressure Injectable Central Venous Catheter
Summary page 1
…Pressure Injectable P1CC with Chlorag'ard Antimicrobial and Antithrombogenic Technology (K 112896) Predicate 2: Arrow Pressure Injectable CVC (K071538) 4. Device Descriition The Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter with Chlorag~ard Antimicro…
Arrow International, Inc.2007Class I

Also cleared against K112896: 3 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K132133CG+ Arrow Jacc Powered by Arrow VPS Stylet Class IArrow International (Subsidiary of Teleflex Inc.)20133

Has anything in its family been recalled? (7 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.

  • K112896Arrw EvolutionArrow International (Subsidiary of Teleflex Inc.) · 2012 · Direct predicate · ◆ on the line of descent in FIG. 11 Class I recall
  • K071538Arrow, Arrowg+Ard and Arrowg+Ard Blue Plus Pressure Injectable Central Venous CatheterArrow International, Inc. · 2007 · Direct predicate · ◆ in the 2007 ancestors bar of FIG. 15 Class I recalls
  • K993691Arrowg +Ard Blue Plus Antimicrobial Multi-Lumen Central Venous CatheterArrow Intl., Inc. · 2000 · 2 generations back · ◆ in the 2000 ancestors bar of FIG. 11 Class I recall
  • K900263Antimicrobial Multi-Lumen Central Venous CatheterArrow Intl., Inc. · 1990 · 2 generations back · ◆ in the 1990 ancestors bar of FIG. 12 Class I recalls
  • K862056[Central Venous][Multi-Lumen] Catheter W/Flex TipArrow Intl., Inc. · 1986 · 2 generations back · ◆ in the 1986 ancestors bar of FIG. 11 Class I recall
  • K132133CG+ Arrow Jacc Powered by Arrow VPS StyletArrow International (Subsidiary of Teleflex Inc.) · 2013 · Cites it directly · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
  • K153423CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex, Inc.) · 2016 · 2 generations on · ◆ in the 2016 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 12 years and passes through 4 companies; a new generation was cleared every 1.2 years on median.
  • 18 of the 33 ancestors have a recall of any class; 5 have a Class I recall.
  • Of its descendants, K132133 (Arrow International (Subsidiary of Teleflex Inc.), 2013) has gone furthest, with 3 descendants of its own.
  • 3 other devices also cite its predicate K112896.

How does its category compare?

All LJS devices

LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · LJS

8in 2025

2007: 142008: 42009: 162010: 92011: 62012: 142013: 142014: 82015: 72016: 92017: 72018: 102020: 22021: 32022: 32023: 42024: 12025: 82026 (partial year): 2
2007high 16 (2009) · low 0 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LJS

171in 2025

2007: 92 days median2008: 97 days median2009: 70 days median2010: 114 days median2011: 55 days median2012: 77 days median2013: 31 days median2014: 47 days median2015: 71 days median2016: 128 days median2017: 101 days median2018: 148 days median2021: 284 days median2022: 177 days median2023: 47 days median2025: 171 days median
2007high 284 (2021) · low 31 (2013)2026

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

Recalls per year · LJS

5in 2023

2008: 12009: 12010: 122011: 42012: 402014: 152015: 22016: 182017: 92018: 32021: 12023: 5, 2 Class I2026 (partial year): 8, 1 Class I
2007high 40 (2012) · low 0 (2007)2026

Class I (3 since 2007) Class II/III not classified

Adverse event reports per year · LJS

4,372in 2025

2007: 3922008: 3692009: 3792010: 4952011: 6962012: 5642013: 6802014: 8422015: 1,3062016: 1,1232017: 2,1002018: 2,3242019: 2,0522020: 2,5392021: 3,0842022: 3,2562023: 2,7992024: 4,2432025: 4,372
2007high 4,372 (2025) · low 369 (2008)2025

MAUDE reports naming product code LJS, 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
200714920392
20084971369
200916701379
2010911412495
20116554696
2012147740564
201314310680
201484715842
201577121,306
20169128181,123
2017710192,100
20181014832,324
20190—02,052
20202—02,539
2021328413,084
2022317703,256
20234475 (2)2,799
20241—04,243
2025817104,372
20262—8 (1)—

What is it indicated for?

The Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter (JACC) with Chlorag~ard® Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term access to the central venous system for intravenous therapy, blood sampling, infusion, pressure injection of contrast media, and allows for central venous pressure monitoring. The maximum pressure of pressure injector equipment used with the Arrow Pressure Injectable JACC…

Read the full statement (159 words)

The Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter (JACC) with Chlorag~ard® Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term access to the central venous system for intravenous therapy, blood sampling, infusion, pressure injection of contrast media, and allows for central venous pressure monitoring. The maximum pressure of pressure injector equipment used with the Arrow Pressure Injectable JACC may not exceed 300 psi. The maximum pressure injection flow rate for the specific lumen being used for pressure injection is printed on the extension line hub.

Chlorag~ard Technology treatment on the external surface of the catheter body as well as the entire fluid pathway of the catheter has been shown to be effective in reducing microbial colonization on catheter surfaces. Antimicrobial effectiveness was evaluated using in vitro and in vivo test methods and no correlation between these testing methods and clinical outcome has currently been ascertained. It is not intended to be used for the treatment of existing infections.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K121501: Arrow Jugular Axillo-Subclavian Central Catheter (Jacc).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K121501

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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