510(k) Report

510(k) · Cleared

Cleared

Apnealink Pro

K131932510(k) TraditionalCleared Nov 8, 2013134-day reviewClass II21 CFR 868.2375

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

Resmed Germany, Inc. · MNR Ventilatory Effort Recorder

Cleared on Nov 8, 2013 as substantially equivalent to K083575 (Resmed Germany, Inc., 2009) after a 134-day review. Its family tree reaches back 8 generations to 1992. 8 later devices descend from it.

Decided
Nov 8, 2013
Review
134 days
Class
Class II
Product code
MNR
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K913396 (1992). 26 ancestors in all, the oldest K914085 (1991). 8 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 2 other ancestors2003: 2 other ancestors2002: 1 other ancestor1998: 2 other ancestors2001: 2 other ancestors1999: 2 other ancestors1992: 3 other ancestors1991: 1 other ancestor1996: 2 other ancestors1995: 1 other ancestor2015: 1 descendant cleared2017: 2 descendants cleared2018: 1 descendant cleared2025: 1 descendant cleared2020: 2 descendants cleared2019: 1 descendant clearedK913396 · Cannula Style Thermocouples · Pro-Tech, Inc. · 1992K982293 · Pressure Transducer Airflow Sensor · Pro-Tech Services, Inc. · 1998K020607 · Sleepflo, Model 101501 · Biomec, Inc. · 2002K030379 · Aplab, Model 801D0030 · Sector Medical Corp. · 2003K040576 · Micromesam Basic-Set · Map Medizintechnik Fur Arzt Und Patient GmbH · 2004K061405 · Apnealink, Model 22302 · Resmed Germany, Inc. · 2006K070263 · Apnealink · Resmed Germany, Inc. · 2007K083575 · Apnealink Plus, Model: 22328 · Resmed Germany, Inc. · 20091990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 3 other ancestors4 generations back: 6 other ancestors5 generations back: 3 other ancestors6 generations back: 2 other ancestors7 generations back: 3 other ancestors 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 3 descendants4 generations forward: 1 descendant5 generations forward: 1 descendant K083575 · Apnealink Plus, Model: 22328 · Resmed Germany, Inc. · 2009K070263 · Apnealink · Resmed Germany, Inc. · 2007K061405 · Apnealink, Model 22302 · Resmed Germany, Inc. · 2006K040576 · Micromesam Basic-Set · Map Medizintechnik Fur Arzt Und Patient GmbH · 2004K030379 · Aplab, Model 801D0030 · Sector Medical Corp. · 2003K020607 · Sleepflo, Model 101501 · Biomec, Inc. · 2002K982293 · Pressure Transducer Airflow Sensor · Pro-Tech Services, Inc. · 1998K913396 · Cannula Style Thermocouples · Pro-Tech, Inc. · 1992−50+5
  1. Root · 8 generations backK913396 Cannula Style ThermocouplesPro-Tech, Inc. · 1992
  2. 7 generations backK982293 Pressure Transducer Airflow SensorPro-Tech Services, Inc. · 1998
  3. 6 generations backK020607 Sleepflo, Model 101501Biomec, Inc. · 2002
  4. 5 generations backK030379 Aplab, Model 801D0030Sector Medical Corp. · 2003
  5. 4 generations backK040576 Micromesam Basic-SetMap Medizintechnik Fur Arzt Und Patient GmbH · 2004
  6. 3 generations backK061405 Apnealink, Model 22302Resmed Germany, Inc. · 2006
  7. 2 generations backK070263 ApnealinkResmed Germany, Inc. · 2007
  8. 1 generation backK083575 Apnealink Plus, Model: 22328Resmed Germany, Inc. · 2009
  9. This deviceK131932 Apnealink ProResmed Germany, Inc. · 2013
  10. Descendant · cites it directly · 7 of its ownK143272 ApneaLink AirResmed Germany, Inc. · 2015
  11. Descendant · 2 generations on · 3 of its ownK163665 MATRx plusZephyr Sleep Technologies · 2017
  12. Descendant · 3 generations on · 2 of its ownK181996 MATRx PlusZephyr Sleep Technologies · 2018
  13. Descendant · 2 generations on · 2 of its ownK172986 Zmachine SynergyConsolidated Research of Richmond, Inc. Dba General Sleep CO · 2017
  14. Descendant · 4 generations on · 1 of its ownK191925 MATRx PlusZephyr Sleep Technologies · 2019

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2015: 12017: 22018: 12019: 12020: 22025: 1
2015high 2 (2017) · low 0 (2016)2026

Most influential descendants

Showing 5 of 8 · See all
  • K143272ApneaLink AirResmed Germany, Inc. · 2015 · cites it directly7descendants
  • K163665MATRx plusZephyr Sleep Technologies · 2017 · 2 generations on3descendants
  • K181996MATRx PlusZephyr Sleep Technologies · 2018 · 3 generations on2descendants
  • K172986Zmachine SynergyConsolidated Research of Richmond, Inc. Dba General Sleep CO · 2017 · 2 generations on2descendants
  • K191925MATRx PlusZephyr Sleep Technologies · 2019 · 4 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K913396Cannula Style ThermocouplesPro-Tech, Inc.1992—
−7K982293Pressure Transducer Airflow SensorPro-Tech Services, Inc.1998—
−6K020607Sleepflo, Model 101501Biomec, Inc.2002—
−5K030379Aplab, Model 801D0030Sector Medical Corp.2003—
−4K040576Micromesam Basic-SetMap Medizintechnik Fur Arzt Und Patient GmbH2004—
−3K061405Apnealink, Model 22302Resmed Germany, Inc.2006—
−2K070263ApnealinkResmed Germany, Inc.2007—
−1K083575Apnealink Plus, Model: 22328Resmed Germany, Inc.2009—
0 (this device)K131932Apnealink ProResmed Germany, Inc.2013—
+1K143272ApneaLink AirResmed Germany, Inc.2015—
+2K163665MATRx plusZephyr Sleep Technologies2017—
+3K181996MATRx PlusZephyr Sleep Technologies2018—
+2K172986Zmachine SynergyConsolidated Research of Richmond, Inc. Dba General Sleep CO2017—
+4K191925MATRx PlusZephyr Sleep Technologies2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199230
199510
199620
199820
199920
200120
200210
200320
200420

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201720
201810
201910
202020
202510
FIG. 1 — Lineage of K131932, 1992–2025Source: 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 MNR? 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 MNR device

  1. #1 K244027 Sansa Hsatscore 18.1 · 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
*K083575Apnealink Plus, Model: 22328
Summary page 1
…rt Recorder Common/Usual Name Ventilatory Effort Recorder Proprietary Name ApneaL-ink Pro Predicate Device ApneaLink Plus (K083575) Reason for submission New device…
Resmed Germany, Inc.2009—

Also cleared against K083575: 2 other devices →

What descends from it? (8)

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

NumberDeviceApplicantDecidedDescendants
K143272ApneaLink AirResmed Germany, Inc.20157

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 21 years and passes through 6 companies; a new generation was cleared every 2.1 years on median.
  • 1 of the 26 ancestors has a recall of any class.
  • Of its descendants, K143272 (Resmed Germany, Inc., 2015) has gone furthest, with 7 descendants of its own.
  • 2 other devices also cite its predicate K083575.

How does its category compare?

All MNR devices

MNR Ventilatory Effort Recorder: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · MNR

10in 2025

2007: 62008: 142009: 82011: 92012: 12013: 42014: 22015: 42016: 32017: 42018: 32019: 82020: 52021: 32022: 72023: 62024: 62025: 102026 (partial year): 5
2007high 14 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MNR

165in 2025

2007: 124 days median2008: 118 days median2009: 89 days median2011: 90 days median2013: 161 days median2015: 229 days median2016: 281 days median2017: 275 days median2018: 147 days median2019: 383 days median2020: 192 days median2021: 137 days median2022: 266 days median2023: 183 days median2024: 217 days median2025: 165 days median2026 (partial year): 227 days median
2007high 383 (2019) · low 89 (2009)2026

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

Recalls per year · MNR

1in 2021

2007: 22009: 12011: 12021: 12026 (partial year): 1
2007high 2 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MNR

43in 2025

2007: 12010: 12011: 12012: 12014: 12015: 42016: 102017: 42018: 22019: 32020: 52021: 52022: 42023: 132024: 112025: 43
2007high 43 (2025) · low 0 (2008)2025

MAUDE reports naming product code MNR, 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
2007612421
20081411800
200988910
20100—01
201199011
20121—01
2013416100
20142—01
2015422904
20163281010
2017427504
2018314702
2019838303
2020519205
2021313715
2022726604
20236183013
20246217011
202510165043
202652271—

What is it indicated for?

The ApneaLink' Pro device is indicated for use by Health Care Professionals (HCP), where it may aid in the diagnosis of sleep disordered breathing for adult patients. ApneaLink Pro records the following data: patient respiratory nasal airflow, snoring, blood oxygen saturation, pulse and respiratory effort during sleep. The device uses these recordings to produce a report for the HCP that may aid in the diagnosis of sleep disordered breathing or for further clinical investigation. The device is intended for home and hospital use under the direction of a HCP.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131932: Apnealink Pro.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131932

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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