510(k) Report

510(k) · Cleared

Cleared

Pilairo Nasal Pillows Mask

K120027510(k) TraditionalCleared Feb 23, 201251-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

Fisher & Paykel Healthcare Limited · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Feb 23, 2012 as substantially equivalent to K063036 (Fisher & Paykel Healthcare, Ltd., 2006) and 1 other predicate after a 51-day review. Its family tree reaches back 8 generations to 1995. 7 later devices descend from it.

Decided
Feb 23, 2012
Review
51 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K952292 (1995). 28 ancestors in all, the oldest K900164 (1990). 7 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor2004: 3 other ancestors2003: 4 other ancestors2002: 3 other ancestors1998: 2 other ancestors1999: 1 other ancestor1996: 2 other ancestors1990: 1 other ancestor2001: 1 other ancestor1994: 1 other ancestor1993: 1 other ancestor2017: 1 descendant cleared2020: 1 descendant cleared2024: 2 descendants cleared2025: 1 descendant cleared2023: 1 descendant cleared2026: 1 descendant clearedK952292 · Puritan-Bennett Companion Nasal Cpap System · Puritan Bennett Corp. · 1995K961626 · Solo Cpap System · Respironics, Inc. · 1996K973161 · Cpap Humidifier (HC 200) · Fisher & Paykel Electronics, Ltd. · 1998K040941 · Cpap Humidifier, Model HC234 (and Related Accessories) · Fisher & Paykel Healthcare, Ltd. · 2004K050904 · Cpap Humidifier, Model HC238JHU · Fisher & Paykel Healthcare, Ltd. · 2005K063036 · Opus HC482 Direct Nasal Mask · Fisher & Paykel Healthcare, Ltd. · 2006K080209 · Fisher and Paykel Healthcare Zest Nasal Mask · Fisher & Paykel Healthcare, Ltd. · 2008K083832 · Zest Nasal Mask · Fisher & Paykel Healthcare, Ltd. · 20091990200020102020
  1. Root · 8 generations backK952292 Puritan-Bennett Companion Nasal Cpap SystemPuritan Bennett Corp. · 1995
  2. 7 generations backK961626 Solo Cpap SystemRespironics, Inc. · 1996
  3. 6 generations backK973161 Cpap Humidifier (HC 200)Fisher & Paykel Electronics, Ltd. · 1998
  4. 5 generations backK040941 Cpap Humidifier, Model HC234 (and Related Accessories)Fisher & Paykel Healthcare, Ltd. · 2004
  5. 4 generations backK050904 Cpap Humidifier, Model HC238JHUFisher & Paykel Healthcare, Ltd. · 2005
  6. 3 generations backK063036 Opus HC482 Direct Nasal MaskFisher & Paykel Healthcare, Ltd. · 2006
  7. 2 generations backK080209 Fisher and Paykel Healthcare Zest Nasal MaskFisher & Paykel Healthcare, Ltd. · 2008
  8. 1 generation backK083832 Zest Nasal MaskFisher & Paykel Healthcare, Ltd. · 2009
  9. This deviceK120027 Pilairo Nasal Pillows MaskFisher & Paykel Healthcare Limited · 2012
  10. Descendant · cites it directly · 6 of its ownK161412 F&P Brevida™ Nasal Pillows MaskFisher & Paykel Healthcare, Ltd. · 2017
  11. Descendant · 2 generations on · 5 of its ownK200089 F&P Evora Nasal Mask Nasal A Model (Small, Medium, Large, Wide), F&P…Fisher & Paykel Healthcare, Ltd. · 2020
  12. Descendant · 3 generations on · 1 of its ownK233415 DELTAWAVE Nasal Pillows SystemRemsleep Holdings · 2024
  13. Descendant · 3 generations on · 1 of its ownK223696 F&P Solo Mask RangeFisher & Paykel Healthcare, Ltd. · 2023
  14. Descendant · 4 generations on · 0 of its ownK253939 DeltaWave Nasal Pillow SystemRemSleep Holdings, Inc. · 2026

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2017: 12020: 12023: 12024: 22025: 12026: 1
2017high 2 (2024) · low 0 (2018)2026

Most influential descendants

Showing 5 of 7 · See all
  • K161412F&P Brevida™ Nasal Pillows MaskFisher & Paykel Healthcare, Ltd. · 2017 · cites it directly6descendants
  • K200089F&P Evora Nasal Mask Nasal A Model (Small, Medium, Large, Wide), F&P Evora Nasal Mask…Fisher & Paykel Healthcare, Ltd. · 2020 · 2 generations on5descendants
  • K233415DELTAWAVE Nasal Pillows SystemRemsleep Holdings · 2024 · 3 generations on1descendant
  • K223696F&P Solo Mask RangeFisher & Paykel Healthcare, Ltd. · 2023 · 3 generations on1descendant
  • K253939DeltaWave Nasal Pillow SystemRemSleep Holdings, Inc. · 2026 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K952292Puritan-Bennett Companion Nasal Cpap SystemPuritan Bennett Corp.1995—
−7K961626Solo Cpap SystemRespironics, Inc.1996—
−6K973161Cpap Humidifier (HC 200)Fisher & Paykel Electronics, Ltd.1998—
−5K040941Cpap Humidifier, Model HC234 (and Related Accessories)Fisher & Paykel Healthcare, Ltd.2004—
−4K050904Cpap Humidifier, Model HC238JHUFisher & Paykel Healthcare, Ltd.2005—
−3K063036Opus HC482 Direct Nasal MaskFisher & Paykel Healthcare, Ltd.2006—
−2K080209Fisher and Paykel Healthcare Zest Nasal MaskFisher & Paykel Healthcare, Ltd.2008—
−1K083832Zest Nasal MaskFisher & Paykel Healthcare, Ltd.2009—
0 (this device)K120027Pilairo Nasal Pillows MaskFisher & Paykel Healthcare Limited2012—
+1K161412F&P Brevida™ Nasal Pillows MaskFisher & Paykel Healthcare, Ltd.2017—
+2K200089F&P Evora Nasal Mask Nasal A Model (Small, Medium, Large, Wide), F&P Evora…Fisher & Paykel Healthcare, Ltd.2020—
+3K233415DELTAWAVE Nasal Pillows SystemRemsleep Holdings2024—
+3K223696F&P Solo Mask RangeFisher & Paykel Healthcare, Ltd.2023—
+4K253939DeltaWave Nasal Pillow SystemRemSleep Holdings, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199310
199410
199620
199820
199910
200110
200230
200340
200430
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
202010
202310
202420
202510
202610
FIG. 1 — Lineage of K120027, 1995–2026Source: 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
Get a 510(k) Report

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
*K063036Opus HC482 Direct Nasal Mask
Summary page 1
…l Pillows Mask Classification Name Non continuous ventilator IPPB (21 CFR § 868.5905, product code EZO) Predicate Devices K063036 Fisher &Paykel Healthcare Opus HC482 Direct Nasal Mask K083832 Fisher & P…
Fisher & Paykel Healthcare, Ltd.2006—
*K083832Zest Nasal Mask
Summary page 1
…05, product code EZO) Predicate Devices K063036 Fisher &Paykel Healthcare Opus HC482 Direct Nasal Mask K083832 Fisher & Paykel Healthcare Zest Nasal Mask (predicate for material biocompatibility)…
Fisher & Paykel Healthcare, Ltd.2009—

Also cleared against K063036: 4 other devices →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K161412F&P Brevida™ Nasal Pillows MaskFisher & Paykel Healthcare, Ltd.20176

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 17 years and passes through 5 companies; a new generation was cleared every 1.7 years on median.
  • 3 of the 28 ancestors have a recall of any class.
  • Of its descendants, K161412 (Fisher & Paykel Healthcare, Ltd., 2017) has gone furthest, with 6 descendants of its own.
  • 4 other devices also cite its predicate K063036.

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?

The F&P Pilairo Nasal Pillows Mask is intended to be used by individuals who have been diagnosed by a physician as requiring CPAP or Bi-Level Ventilator treatment. The F&P Pilairo Nasal Pillows Mask is intended for single-patient adult use in the home and multiple-patient adult use in the hospital or other clinical setting where proper disinfection of the device can occur between patient uses.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K120027: Pilairo Nasal Pillows Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K120027

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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