510(k) Report

510(k) · Cleared

Cleared

iCodeConnect

K160127510(k) TraditionalCleared Nov 10, 2016295-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

3B Medical, Inc. · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Nov 10, 2016 as substantially equivalent to K093684 (Resmed, Ltd., 2010) after a 295-day review. Its family tree reaches back 8 generations to 1997.

Decided
Nov 10, 2016
Review
295 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K971260 (1997). 21 ancestors in all, the oldest K930656 (1994). No later device cites it as a predicate yet.

  1. Root · 8 generations backK971260 Sullivan Humidaire Heated HumidifierResmed Corp · 1997
  2. 7 generations backK013909 S7 Elite CP AP SystemResmed Corp · 2002
  3. 6 generations backK024191 S7 Elite and Autoset Spirit Cpap Systems with ReslinkResmed, Ltd. · 2003
  4. 5 generations backK033841 Resmed S8 Prime Cpap SystemResmed, Ltd. · 2004 · Recalled
  5. 4 generations backK041209 Resmed S8 Pioneer Cpap SystemResmed, Ltd. · 2004 · Recalled
  6. 3 generations backK050775 ResscanResmed, Ltd. · 2005
  7. 2 generations backK082983 Resscan-ProResmed, Ltd. · 2009
  8. 1 generation backK093684 Easycare OnlineResmed, Ltd. · 2010
  9. This deviceK160127 iCodeConnect3B Medical, Inc. · 2016
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K971260Sullivan Humidaire Heated HumidifierResmed Corp1997—
−7K013909S7 Elite CP AP SystemResmed Corp2002—
−6K024191S7 Elite and Autoset Spirit Cpap Systems with ReslinkResmed, Ltd.2003—
−5K033841Resmed S8 Prime Cpap SystemResmed, Ltd.20041
−4K041209Resmed S8 Pioneer Cpap SystemResmed, Ltd.20041
−3K050775ResscanResmed, Ltd.2005—
−2K082983Resscan-ProResmed, Ltd.2009—
−1K093684Easycare OnlineResmed, Ltd.2010—
0 (this device)K160127iCodeConnect3B Medical, Inc.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199610
199810
200230
200310
200420
200510
200610
200710
200910
FIG. 1 — Lineage of K160127, 1997–2016Source: 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.

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
*K093684Easycare Online
Summary page 5
…CFR 878.5905 Products Code BZD Medical Specialties Anesthesiology Predicate Device(s) EasyCare Online (K093684) Reason for Submission: New Device Intended Use iCodeConnect, in conjunction with a Luna CPA…
Resmed, Ltd.2010—

Also cleared against K093684: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 19 years and passes through 3 companies; a new generation was cleared every 1.1 years on median.
  • 2 of the 21 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K093684.

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. 2016, 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?

iCodeConnect, in conjunction with a Luna CPAP or Auto-CPAP device, is intended for use in treating obstructive sleep apnea (OSA) on adult patients (>30 kg).

iCodeConnect is intended to augment the standard follow-up care of patients diagnosed with obstructive sleep apnea by displaying usage and therapeutic information that has been transmitted from the patient's Luna CPAP or Auto-CPAP therapy device located in the home to the clinician or healthcare professional. iCodeConnect also provides remote settings capabilities.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K160127: iCodeConnect.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K160127

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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