510(k) Report

510(k) · Decided

Decided

Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube

K160509510(k) TraditionalDecided May 18, 2017449-day reviewClass II21 CFR 876.5980

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

Cook Incorporated · KNT Tubes, Gastrointestinal (And Accessories)

Cleared on May 18, 2017 as substantially equivalent to K043203 (Wilson-Cook Medical, Inc., 2005) after a 449-day review. Its family tree reaches back 2 generations to 1987. 1 later device descends from it.

Decided
May 18, 2017
Review
449 days
Class
Class II
Product code
KNT
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K874393 (1987). 1 later device descends from it, 1 citing it directly.

  1. Root · 2 generations backK874393 Enteral Feeding TubeWilson-Cook Medical, Inc. · 1987 · Recalled
  2. 1 generation backK043203 Wilson-Cook Enteral Feeding Tube, Tiger Tube Enteral Feeding TubeWilson-Cook Medical, Inc. · 2005 · Recalled
  3. This deviceK160509 Tiger 2 Self-Advancing Nasal Jejunal Feeding TubeCook Incorporated · 2017
  4. Descendant · cites it directly · 0 of its ownK190084 McLean-Ring Enteral Feeding Tube SetCook Incorporated · 2019

Most influential descendants

Showing 1 of 1 · See all
  • K190084McLean-Ring Enteral Feeding Tube SetCook Incorporated · 2019 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K874393Enteral Feeding TubeWilson-Cook Medical, Inc.19871
−1K043203Wilson-Cook Enteral Feeding Tube, Tiger Tube Enteral Feeding TubeWilson-Cook Medical, Inc.20051
0 (this device)K160509Tiger 2 Self-Advancing Nasal Jejunal Feeding TubeCook Incorporated2017—
+1K190084McLean-Ring Enteral Feeding Tube SetCook Incorporated2019—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
FIG. 1 — Lineage of K160509, 1987–2019Source: 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 KNT? 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 KNT device

  1. #1 K261890 52Fr ViSiGi LUX™; 52Fr ViSiGi 3D®score 12.7 · 4 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? (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
*K043203Wilson-Cook Enteral Feeding Tube, Tiger Tube Enteral Feeding Tube
Summary page 4
…, is substantially equivalent to the predicate device, the Wilson-Cook Nasal Jejunal Feeding Tubes and Nasal Jejunal Feeding Tube with Flaps, cleared under 510(k) number K043203. Device Description: The Tiger 2™ Self-Advancing Nasal Jejunal Feeding Tube consists of a 14 Fr polyether-urethane tube manufac…
Wilson-Cook Medical, Inc.20051

Also cleared against K043203: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K190084McLean-Ring Enteral Feeding Tube SetCook Incorporated20190

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 30 years and passes through 2 companies; a new generation was cleared every 17.4 years on median.
  • 2 of the 2 ancestors have a recall of any class.
  • Of its descendants, K190084 (Cook Incorporated, 2019) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K043203.

How does its category compare?

All KNT devices

KNT Tubes, Gastrointestinal (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · KNT

4in 2025

2007: 102008: 102009: 112010: 122011: 72012: 122013: 72014: 162015: 102016: 62017: 92018: 72019: 102020: 52021: 62022: 72023: 52024: 92025: 42026 (partial year): 3
2007high 16 (2014) · low 4 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KNT

136in 2025

2007: 118 days median2008: 115 days median2009: 102 days median2010: 104 days median2011: 211 days median2012: 107 days median2013: 128 days median2014: 259 days median2015: 140 days median2016: 99 days median2017: 247 days median2018: 149 days median2019: 126 days median2020: 102 days median2021: 121 days median2022: 110 days median2023: 162 days median2024: 103 days median2025: 136 days median2026 (partial year): 105 days median
2007high 259 (2014) · low 99 (2016)2026

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

Recalls per year · KNT

13in 2025

2007: 12008: 822009: 92010: 32011: 22012: 12015: 12016: 32017: 42018: 22019: 22020: 12021: 22022: 1, 1 Class I2023: 22025: 132026 (partial year): 20
2007high 82 (2008) · low 0 (2013)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · KNT

1,451in 2025

2007: 3002008: 8672009: 8182010: 5172011: 5312012: 5282013: 7472014: 1,0302015: 1,0482016: 1,2512017: 1,6722018: 1,9012019: 1,8382020: 1,6412021: 1,6552022: 1,6502023: 1,8632024: 1,3442025: 1,451
2007high 1,901 (2018) · low 300 (2007)2025

MAUDE reports naming product code KNT, 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
2007101181300
20081011582867
2009111029818
2010121043517
201172112531
2012121071528
201371280747
20141625901,030
20151014011,048
201669931,251
2017924741,672
2018714921,901
20191012621,838
2020510211,641
2021612121,655
202271101 (1)1,650
2023516221,863
2024910301,344
20254136131,451
2026310520—

What is it indicated for?

The Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube is intended to provide short-term enteral access for delivery of nutrition and/or medications to the small bowel in patients older than 12 years old.

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. “K160509: Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K160509

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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