510(k) Report

510(k) · Cleared

Cleared

The Sherlock 3CG Tip Confirmation System (TCS)

K113808510(k) TraditionalCleared Mar 19, 201287-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

C.R. Bard, Inc. · LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

Cleared on Mar 19, 2012 as substantially equivalent to K112744 (C.R. Bard, Inc., 2011) and 1 other predicate after an 87-day review. Its family tree reaches back 10 generations to 2000. 6 later devices descend from it.

Decided
Mar 19, 2012
Review
87 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 K823434 (1982). 6 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2006: 1 other ancestor2004: 1 other ancestor2003: 1 other ancestor1984: 1 other ancestor2002: 2 other ancestors2000: 1 other ancestor1997: 1 other ancestor1995: 2 other ancestors1992: 2 other ancestors1996: 2 other ancestors1994: 3 other ancestors1993: 1 other ancestor1991: 2 other ancestors1986: 1 other ancestor1982: 1 other ancestor2014: 1 descendant cleared2015: 1 descendant cleared2018: 1 descendant cleared2025: 2 descendants cleared2026: 1 descendant clearedK001901 · 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. · 2003K034019 · Poly Per-Q-Cath Picc Catheters · C.R. Bard, Inc. · 2004 · recalledK060341 · Sherlock Tip Location System (TLS) · C.R. Bard, Inc. · 2006K063240 · Sherlock TLS Stylet, Sherlock TLS Detector · C.R. Bard, Inc. · 2006 · recalledK081625 · Flowpicc Stylet · Vasonova, Inc. · 2008K091324 · Sherlock 3CG Tip Positioning System, Sherlock 3CG Tip Positioning System Stylet · C.R. Bard, Inc. · 2009 · recalledK093775 · Evguide Tip Location System · Romedex International Srl · 2010K112744 · Sapiens Tip Confirmation System · C.R. Bard, Inc. · 201119801990200020102020
  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 backK091324 Sherlock 3CG Tip Positioning System, Sherlock 3CG Tip Positioning…C.R. Bard, Inc. · 2009 · Recalled
  4. 2 generations backK093775 Evguide Tip Location SystemRomedex International Srl · 2010
  5. 1 generation backK112744 Sapiens Tip Confirmation SystemC.R. Bard, Inc. · 2011
  6. This deviceK113808 The Sherlock 3CG Tip Confirmation System (TCS)C.R. Bard, Inc. · 2012
  7. Descendant · cites it directly · 4 of its ownK141634 Nautilus DeltaRomedex International Srl · 2015
  8. Descendant · 2 generations on · 2 of its ownK241910 Neonav ECG Tip Location SystemNavi Medical Technologies · 2025
  9. Descendant · cites it directly · 2 of its ownK140345 The Sherlock 3CG Tip Confirmation System (TCS)C.R. Bard, Inc. · 2014
  10. Descendant · 2 generations on · 1 of its ownK180560 Sherlock 3CG+ T ip Confirmation SystemC.R. Bard, Inc. · 2018
  11. Descendant · 3 generations on · 0 of its ownK260929 Neonav ECG Tip Location SystemNavi Medical Technologies · 2026
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 backK034019 Poly Per-Q-Cath Picc CathetersC.R. Bard, Inc. · 2004 · Recalled
  5. 6 generations backK060341 Sherlock Tip Location System (TLS)C.R. Bard, Inc. · 2006
  6. 5 generations backK063240 Sherlock TLS Stylet, Sherlock TLS DetectorC.R. Bard, Inc. · 2006 · Recalled
  7. 4 generations backK081625 Flowpicc StyletVasonova, Inc. · 2008
  8. 3 generations backK091324 Sherlock 3CG Tip Positioning System, Sherlock 3CG Tip Positioning…C.R. Bard, Inc. · 2009 · Recalled
  9. 2 generations backK093775 Evguide Tip Location SystemRomedex International Srl · 2010
  10. 1 generation backK112744 Sapiens Tip Confirmation SystemC.R. Bard, Inc. · 2011
  11. This deviceK113808 The Sherlock 3CG Tip Confirmation System (TCS)C.R. Bard, Inc. · 2012

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2014: 12015: 12018: 12025: 22026: 1
2014high 2 (2025) · low 0 (2016)2026

Most influential descendants

Showing 5 of 6 · See all
  • K141634Nautilus DeltaRomedex International Srl · 2015 · cites it directly4descendants
  • K241910Neonav ECG Tip Location SystemNavi Medical Technologies · 2025 · 2 generations on2descendants
  • K140345The Sherlock 3CG Tip Confirmation System (TCS)C.R. Bard, Inc. · 2014 · cites it directly2descendants
  • K180560Sherlock 3CG+ T ip Confirmation SystemC.R. Bard, Inc. · 2018 · 2 generations on1descendant
  • K260929Neonav ECG Tip Location SystemNavi Medical Technologies · 2026 · 3 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—
−7K034019Poly Per-Q-Cath Picc CathetersC.R. Bard, Inc.20041
−6K060341Sherlock Tip Location System (TLS)C.R. Bard, Inc.2006—
−5K063240Sherlock TLS Stylet, Sherlock TLS DetectorC.R. Bard, Inc.200618
−4K081625Flowpicc StyletVasonova, Inc.2008—
−3K091324Sherlock 3CG Tip Positioning System, Sherlock 3CG Tip Positioning System StyletC.R. Bard, Inc.200911
−2K093775Evguide Tip Location SystemRomedex International Srl2010—
−1K112744Sapiens Tip Confirmation SystemC.R. Bard, Inc.2011—
0 (this device)K113808The Sherlock 3CG Tip Confirmation System (TCS)C.R. Bard, Inc.2012—
+1K141634Nautilus DeltaRomedex International Srl2015—
+2K241910Neonav ECG Tip Location SystemNavi Medical Technologies2025—
+1K140345The Sherlock 3CG Tip Confirmation System (TCS)C.R. Bard, Inc.2014—
+2K180560Sherlock 3CG+ T ip Confirmation SystemC.R. Bard, Inc.2018—
+3K260929Neonav ECG Tip Location SystemNavi Medical Technologies2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
198410
198610
199120
199220
199310
199430
199520
199620
199710
200010
200220
200310
200410
200610
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201510
201810
202520
202610
FIG. 1 — Lineage of K113808, 2000–2026Source: 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 LJS? 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
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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
*K112744Sapiens Tip Confirmation System
Summary page 1
…US - Percutaneous, implanted, long-term Intravascular catheters Premarket Notification: K1 12744, concurrence date 20 October 2011 Manufacturer: Bard Access Systems, Inc. Predicate…
C.R. Bard, Inc.2011—
*K091324Sherlock 3CG Tip Positioning System, Sherlock 3CG Tip Positioning System Stylet
Summary page 1
…US - Percutaneous, implanted, long-term Intravascular catheters Premarket Notification: K091324, concurrence date 07 August 2009 Manufacturer: Bard Access Systems, Inc. Device T…
C.R. Bard, Inc.200911

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K141634Nautilus DeltaRomedex International Srl20154
K140345The Sherlock 3CG Tip Confirmation System (TCS)C.R. Bard, Inc.20142

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 12 years and passes through 3 companies; a new generation was cleared every 12 months on median.
  • 7 of the 33 ancestors have a recall of any class.
  • Of its descendants, K141634 (Romedex International Srl, 2015) has gone furthest, with 4 descendants of its own.

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 Sherlock 3 CG TM Tip Confirmation System (TCS) is indicated for guidance and positioning of Peripherally Inserted Central Catheters (PICCs). The Sherlock 3CG TCS provides real-time PICC tip location information by using passive magnet tracking and the patient's cardiac electrical activity (ECG). When relying on the patient's ECG signal, the Sherlock 3CG TOS is indicated for use as an alternative method to chest X-ray and fluoroscopy for P1CC tip…

Read the full statement (134 words)

The Sherlock 3 CG TM Tip Confirmation System (TCS) is indicated for guidance and positioning of Peripherally Inserted Central Catheters (PICCs). The Sherlock 3CG TCS provides real-time PICC tip location information by using passive magnet tracking and the patient's cardiac electrical activity (ECG). When relying on the patient's ECG signal, the Sherlock 3CG TOS is indicated for use as an alternative method to chest X-ray and fluoroscopy for P1CC tip placement confirmation in adult patients.

Limiting but not contraindicated situations for this technique are in patients where alterations of cardiac rhythm change the presentation of the P wave as in atrial fibrillation, atrial flutter, severe tachycardia, and pacemaker driven rhythm. In such patients, who are easily identifiable prior to catheter insertion, the use of an additional method is required to confirm P1CC tip location:

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K113808: The Sherlock 3CG Tip Confirmation System (TCS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K113808

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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