510(k) Report

510(k) · Cleared

Cleared

Flexifit HC432 Full Face Mask

K061236510(k) TraditionalCleared Aug 29, 2006118-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, Ltd. · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Aug 29, 2006 as substantially equivalent to K040506 (Fisher & Paykel Healthcare, Ltd., 2004) and 1 other predicate after a 118-day review. Its family tree reaches back 4 generations to 2001. 25 later devices descend from it.

Decided
Aug 29, 2006
Review
118 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K003894 (2001). 7 ancestors in all, the oldest K982530 (1998). 25 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor1999: 1 other ancestor1998: 1 other ancestor2006: 1 descendant cleared2011: 1 descendant cleared2008: 1 descendant cleared2009: 1 descendant cleared2012: 5 descendants cleared2013: 3 descendants cleared2014: 1 descendant cleared2017: 1 descendant cleared2016: 1 descendant cleared2020: 2 descendants cleared2019: 1 descendant cleared2023: 2 descendants cleared2024: 2 descendants cleared2025: 1 descendant cleared2022: 1 descendant cleared2026: 1 descendant clearedK003894 · Oracle Oral Mask · Fisher & Paykel Healthcare, Ltd. · 2001 · recalledK023559 · Fisher & Paykel Healthecare Oracle Oral Mask · Fisher & Paykel Healthcare, Ltd. · 2003×2: 2 generations cleared close together, K033087 (2004), K040506 (2004) 1995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 2 other ancestors 1 generation forward: 3 descendants2 generations forward: 4 descendants3 generations forward: 6 descendants4 generations forward: 4 descendants5 generations forward: 5 descendants6 generations forward: 3 descendants K040506 · Flexifil Series HC431 Full Face Mask, Model HC431A · Fisher & Paykel Healthcare, Ltd. · 2004 · recalledK033087 · Oracle Oral Mask, Model HC451A · Fisher & Paykel Healthcare, Ltd. · 2004 · recalledK023559 · Fisher & Paykel Healthecare Oracle Oral Mask · Fisher & Paykel Healthcare, Ltd. · 2003K003894 · Oracle Oral Mask · Fisher & Paykel Healthcare, Ltd. · 2001 · recalled0+5
  1. Root · 4 generations backK003894 Oracle Oral MaskFisher & Paykel Healthcare, Ltd. · 2001 · Recalled
  2. 3 generations backK023559 Fisher & Paykel Healthecare Oracle Oral MaskFisher & Paykel Healthcare, Ltd. · 2003
  3. 2 generations backK033087 Oracle Oral Mask, Model HC451AFisher & Paykel Healthcare, Ltd. · 2004 · Recalled
  4. 1 generation backK040506 Flexifil Series HC431 Full Face Mask, Model HC431AFisher & Paykel Healthcare, Ltd. · 2004 · Recalled
  5. This deviceK061236 Flexifit HC432 Full Face MaskFisher & Paykel Healthcare, Ltd. · 2006
  6. Descendant · cites it directly · 24 of its ownK063036 Opus HC482 Direct Nasal MaskFisher & Paykel Healthcare, Ltd. · 2006
  7. Descendant · cites it directly · 15 of its ownK080209 Fisher and Paykel Healthcare Zest Nasal MaskFisher & Paykel Healthcare, Ltd. · 2008
  8. Descendant · 2 generations on · 14 of its ownK083832 Zest Nasal MaskFisher & Paykel Healthcare, Ltd. · 2009
  9. Descendant · 2 generations on · 7 of its ownK120027 Pilairo Nasal Pillows MaskFisher & Paykel Healthcare Limited · 2012
  10. Descendant · 3 generations on · 6 of its ownK161412 F&P Brevida™ Nasal Pillows MaskFisher & Paykel Healthcare, Ltd. · 2017

Showing 5 of 25 descendants. See all descendants

Descendants cleared per year

2006: 12008: 12009: 12011: 12012: 52013: 32014: 12016: 12017: 12019: 12020: 22022: 12023: 22024: 22025: 12026: 1
2006high 5 (2012) · low 0 (2007)2026

Most influential descendants

Showing 5 of 25 · See all
  • K063036Opus HC482 Direct Nasal MaskFisher & Paykel Healthcare, Ltd. · 2006 · cites it directly24descendants
  • K080209Fisher and Paykel Healthcare Zest Nasal MaskFisher & Paykel Healthcare, Ltd. · 2008 · cites it directly15descendants
  • K083832Zest Nasal MaskFisher & Paykel Healthcare, Ltd. · 2009 · 2 generations on14descendants
  • K120027Pilairo Nasal Pillows MaskFisher & Paykel Healthcare Limited · 2012 · 2 generations on7descendants
  • K161412F&P Brevida™ Nasal Pillows MaskFisher & Paykel Healthcare, Ltd. · 2017 · 3 generations on6descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K003894Oracle Oral MaskFisher & Paykel Healthcare, Ltd.20016
−3K023559Fisher & Paykel Healthecare Oracle Oral MaskFisher & Paykel Healthcare, Ltd.2003—
−2K033087Oracle Oral Mask, Model HC451AFisher & Paykel Healthcare, Ltd.20046
−1K040506Flexifil Series HC431 Full Face Mask, Model HC431AFisher & Paykel Healthcare, Ltd.20046
0 (this device)K061236Flexifit HC432 Full Face MaskFisher & Paykel Healthcare, Ltd.2006—
+1K063036Opus HC482 Direct Nasal MaskFisher & Paykel Healthcare, Ltd.2006—
+1K080209Fisher and Paykel Healthcare Zest Nasal MaskFisher & Paykel Healthcare, Ltd.2008—
+2K083832Zest Nasal MaskFisher & Paykel Healthcare, Ltd.2009—
+2K120027Pilairo Nasal Pillows MaskFisher & Paykel Healthcare Limited2012—
+3K161412F&P Brevida™ Nasal Pillows MaskFisher & Paykel Healthcare, Ltd.2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
199910
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
200810
200910
201110
201250
201330
201410
201610
201710
201910
202020
202210
202320
202420
202510
202610
FIG. 1 — Lineage of K061236, 2001–2026Source: 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
*K040506Flexifil Series HC431 Full Face Mask, Model HC431A
Summary page 1
…name Full Face Mask Classification Non continuous ventilator IPPB name (21 CFR § 868.5905, product code BZD) K040506 Fisher & Paykel Healthcare Flexifit HC431 Face Mask Predicate K033087 Fisher & Paykel Healthcare Oracle Oral Mask (p…
Fisher & Paykel Healthcare, Ltd.20046
*K033087Oracle Oral Mask, Model HC451A
Summary page 1
…PB name (21 CFR § 868.5905, product code BZD) K040506 Fisher & Paykel Healthcare Flexifit HC431 Face Mask Predicate K033087 Fisher & Paykel Healthcare Oracle Oral Mask (predicate for material biocompatibility)…
Fisher & Paykel Healthcare, Ltd.20046

Also cleared against K040506: 4 other devices →

What descends from it? (25)

See all 25

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K063036Opus HC482 Direct Nasal MaskFisher & Paykel Healthcare, Ltd.200624
K080209Fisher and Paykel Healthcare Zest Nasal MaskFisher & Paykel Healthcare, Ltd.200815
K103786Zest Petite Nasal MaskFisher & Paykel Healthcare, Ltd.20110

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 5 years and passes through 1 company; a new generation was cleared every 2.0 years on median.
  • 3 of the 7 ancestors have a recall of any class.
  • Of its descendants, K063036 (Fisher & Paykel Healthcare, Ltd., 2006) has gone furthest, with 24 descendants of its own.
  • 4 other devices also cite its predicate K040506.

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.

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 Flexifit HC432 Full Face Mask is intended for multiple patient or single patient adult use

by individuals who have been diagnosed by a physician as requiring CPAP or Bilevel ventilator

treatment in the home, hospital or other clinical setting.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K061236: Flexifit HC432 Full Face Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K061236

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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