510(k) Report

510(k) · Cleared

Cleared

Rusch Tracflex Plus Pediatric Tracheostomy Tube Set

K133173510(k) TraditionalCleared May 23, 2014218-day reviewClass II21 CFR 868.5800

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

Teleflexmedical, Inc. · JOH Tube Tracheostomy And Tube Cuff

Cleared on May 23, 2014 as substantially equivalent to K023918 (Rusch Intl., 2003) and 1 other predicate after a 218-day review. Its family tree reaches back 4 generations to 1994. 1 of the 9 devices in its family, counting itself, has a Class I recall.

Decided
May 23, 2014
Review
218 days
Class
Class II
Product code
JOH
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K934465 (1994). 8 ancestors in all, the oldest K913270 (1991). No later device cites it as a predicate yet. 1 of the 9 devices in this family, counting this one, has a Class I recall.

  1. Root · 4 generations backK934465 Dic Tracheostomy Tube and Portex Blue LineSmiths Industries Medical Systems, Inc. · 1994 · Recalled
  2. 3 generations backK955564 Rusch Ultra Tracheoflex Tracheostomy Set, Cuffed, SterileRusch, Inc. · 1996
  3. 2 generations backK964056 Rusch Ultra Tracheoflex Fenestrated Kit Cuffed,Uncuffed/ Rusch…Rusch Intl. · 1997 · Recalled (Class I)
  4. 1 generation backK122235 Rusch Tracflex Plus Tracheostomy Tube SetTeleflexmedical, Inc. · 2013
  5. This deviceK133173 Rusch Tracflex Plus Pediatric Tracheostomy Tube SetTeleflexmedical, Inc. · 2014

Class I recalls in this family

View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K934465Dic Tracheostomy Tube and Portex Blue LineSmiths Industries Medical Systems, Inc.19942
−3K955564Rusch Ultra Tracheoflex Tracheostomy Set, Cuffed, SterileRusch, Inc.1996—
−2K964056Rusch Ultra Tracheoflex Fenestrated Kit Cuffed,Uncuffed/ Rusch Tracheoflex…Rusch Intl.1997Class I
−1K122235Rusch Tracflex Plus Tracheostomy Tube SetTeleflexmedical, Inc.2013—
0 (this device)K133173Rusch Tracflex Plus Pediatric Tracheostomy Tube SetTeleflexmedical, Inc.2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199120
199810
200310
FIG. 1 — Lineage of K133173, 1994–2014Source: 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.

1 device in this family has 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 JOH device

  1. #1 K251313 Shiley™ Adult Flexible Tracheostomy Tube XLT…score 11.2 · 3 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
*K023918Rusch Crystal Clear Tracheostomy Sets, Cuffed and Cuffless
Summary page 2
…Features Proposed TracFlex Plus Predicate Crystal Clear Predicate (for reference) Pediatric K023918 TracFlex Plus __________________ __________________K122235…
Rusch Intl.20032
*K122235Rusch Tracflex Plus Tracheostomy Tube Set
Summary page 2
…Pediatric K023918 TracFlex Plus __________________ __________________K122235 Device Rusch TracFlex Plus Rusch Crystal Clear Rusch TracFlex Plus…
Teleflexmedical, Inc.2013—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (1 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.

  • K964056Rusch Ultra Tracheoflex Fenestrated Kit Cuffed,Uncuffed/ Rusch Tracheoflex Tracheostomy Kit Uncuffed SterileRusch Intl. · 1997 · 2 generations back · ◆ on the line of descent in FIG. 11 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 2.5 years on median.
  • 4 of the 8 ancestors have a recall of any class; 1 has a Class I recall.

How does its category compare?

All JOH devices

JOH Tube Tracheostomy And Tube Cuff: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · JOH

1in 2025

2007: 12008: 22009: 12010: 22012: 12013: 32014: 32015: 32016: 12017: 12018: 32019: 22020: 12021: 22025: 1
2007high 3 (2013) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JOH

137in 2018

2013: 407 days median2014: 218 days median2015: 179 days median2018: 137 days median
2007high 407 (2013) · low 137 (2018)2026

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

Recalls per year · JOH

1in 2023

2007: 12009: 12010: 732011: 42016: 2, 1 Class I2020: 12023: 12026 (partial year): 1
2007high 73 (2010) · low 0 (2008)2026

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

Adverse event reports per year · JOH

986in 2025

2007: 1672008: 1022009: 1952010: 1,2702011: 5872012: 5002013: 5442014: 5062015: 5082016: 5722017: 4412018: 8122019: 1,0192020: 7912021: 1,0412022: 1,6322023: 1,2332024: 1,1032025: 986
2007high 1,632 (2022) · low 102 (2008)2025

MAUDE reports naming product code JOH, 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
20071—1167
20082—0102
20091—1195
20102—731,270
20110—4587
20121—0500
201334070544
201432180506
201531790508
20161—2 (1)572
20171—0441
201831370812
20192—01,019
20201—1791
20212—01,041
20220—01,632
20230—11,233
20240—01,103
20251—0986
20260—1—

What is it indicated for?

The Rusch TracFlex Plus Pediatric Tracheostomy Tube Set is used in airway management of tracheostomized patients.

Patient Population: Pediatric Patients per below:

Pediatric Subgroup Approximate Age Range

Neonate/Newborn Birth to 28 days

Infant 29 days to < 2 years

Child 2 years to <12 years

Adolescent 12 years to < 18 years

Transitional Adolescent A 18 years to <21 years

Environment of use: Home, Hospital and Sub-acute Institutions

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K133173: Rusch Tracflex Plus Pediatric Tracheostomy Tube Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K133173

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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