510(k) Report

510(k) · Cleared

Cleared

Easycare TX System (Connexuns)

K113780510(k) TraditionalCleared Apr 20, 2012120-day reviewClass II21 CFR 868.5905

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

Resmed, Ltd. · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Apr 20, 2012 as substantially equivalent to K092026 (Resmed, Ltd., 2009) after a 120-day review. Its family tree reaches back 4 generations to 1996. 1 later device descends from it.

Decided
Apr 20, 2012
Review
120 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K961783 (1996). 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK961783 Sullivan Vpap II ST Nasal Vpap SystemResmed, Ltd. · 1996
  2. 3 generations backK040944 Rescontrol IIResmed, Ltd. · 2004
  3. 2 generations backK072615 TxcontrolResmed, Ltd. · 2008
  4. 1 generation backK092026 Easycare TX, TX LinkResmed, Ltd. · 2009
  5. This deviceK113780 Easycare TX System (Connexuns)Resmed, Ltd. · 2012
  6. Descendant · cites it directly · 0 of its ownK241939 EasyCare Tx 2Resmed Corp · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K241939EasyCare Tx 2Resmed Corp · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K961783Sullivan Vpap II ST Nasal Vpap SystemResmed, Ltd.1996—
−3K040944Rescontrol IIResmed, Ltd.2004—
−2K072615TxcontrolResmed, Ltd.2008—
−1K092026Easycare TX, TX LinkResmed, Ltd.2009—
0 (this device)K113780Easycare TX System (Connexuns)Resmed, Ltd.2012—
+1K241939EasyCare Tx 2Resmed Corp2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K113780, 1996–2024Source: 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 BZD? 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 BZD device

  1. #1 K250624 myAirscore 15.7 · 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? (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
*K092026Easycare TX, TX Link
Summary page 1
…lt~sual Name Non-continuous ventilator (IPPB) Proprietary Name EasyCare Tx System Predicate Device(s) EasyCare Tx System (K092026) Reason for submission New Device Th March 2012Pae4 RESMED The EasyCare Tx System comprises of…
Resmed, Ltd.2009—
†K971813EMBLAFerguson Medical1998—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K241939EasyCare Tx 2Resmed Corp20240

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 16 years and passes through 1 company; a new generation was cleared every 3.6 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K241939 (Resmed Corp, 2024) has gone furthest, with 0 descendants of its own.

How does its category compare?

All BZD devices

BZD Ventilator, Non-Continuous (Respirator): FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · BZD

7in 2025

2007: 212008: 172009: 232010: 122011: 232012: 212013: 232014: 142015: 112016: 122017: 52018: 52019: 62020: 62021: 62022: 42023: 52024: 102025: 72026 (partial year): 10
2007high 23 (2009) · low 4 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BZD

189in 2025

2007: 83 days median2008: 108 days median2009: 90 days median2010: 122 days median2011: 125 days median2012: 133 days median2013: 127 days median2014: 172 days median2015: 224 days median2016: 217 days median2017: 221 days median2018: 280 days median2019: 231 days median2020: 137 days median2021: 192 days median2022: 253 days median2023: 204 days median2024: 132 days median2025: 189 days median2026 (partial year): 214 days median
2007high 280 (2018) · low 83 (2007)2026

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

Recalls per year · BZD

8in 2023

2007: 292008: 22009: 12011: 12019: 4, 4 Class I2023: 8, 7 Class I2026 (partial year): 2, 2 Class I
2007high 29 (2007) · low 0 (2010)2026

Class I (13 since 2007) Class II/III not classified

Adverse event reports per year · BZD

60,279in 2025

2007: 652008: 672009: 1472010: 1432011: 1892012: 1392013: 822014: 862015: 1142016: 1182017: 1482018: 1012019: 1882020: 1262021: 6,0662022: 90,7682023: 27,9872024: 68,2622025: 60,279
2007high 90,768 (2022) · low 65 (2007)2025

MAUDE reports naming product code BZD, 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
200721832965
200817108267
200923901147
2010121220143
2011231251189
2012211330139
201323127082
201414172086
2015112240114
2016122170118
201752210148
201852800101
201962314 (4)188
202061370126
2021619206,066
20224253090,768
202352048 (7)27,987
202410132068,262
20257189060,279
2026102142 (2)—

What is it indicated for?

EasyCare Tx is intended to be used with ResMed compatible therapy devices via the Tx Link. EasyCare Tx provides real-time data and treatment settings display, and can also provide therapy device setting changes remotely.

EasyCare Tx is intended to be used in a clinical environment.

The Tx Link is intended to provide connectivity between ResMed EasyCare Tx software and ResMed compatible therapy devices. The Tx Link relays real-time signals measured by the ResMed compatible therapy device to a polysomnograph (PSG).

The Tx Link is intended to be used in a clinical environment.

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. “K113780: Easycare TX System (Connexuns).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113780

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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