510(k) Report

510(k) · Cleared

Cleared

Nasal Mask, Nasal Mask, Full Face Mask

K133009510(k) TraditionalCleared Apr 23, 2014210-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

BMC Medical Co., Ltd. · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Apr 23, 2014 as substantially equivalent to K092835 (Respironics Inc., Sleep & Home Respiratory Group, 2010) and 2 other predicates after a 210-day review. Its family tree reaches back 6 generations to 1998. 1 later device descends from it.

Decided
Apr 23, 2014
Review
210 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
3

Its longest line of descent runs back 6 generations to K982530 (1998). 22 ancestors in all, the oldest K833786 (1983). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2003: 2 other ancestors2008: 1 other ancestor1999: 2 other ancestors1996: 3 other ancestors2002: 2 other ancestors2000: 1 other ancestor1998: 1 other ancestor1988: 1 other ancestor1983: 1 other ancestor1990: 1 other ancestor2017: 1 descendant clearedK982530 · Sullivan Mirage Full Face Mask · Resmed, Ltd. · 1998K023244 · Mirage Full Face Mask Series 2 · Resmed, Ltd. · 2002K032916 · Mirage Activa Mask · Resmed, Ltd. · 2003K042403 · Mirage Swift · Resmed, Ltd. · 2004K063122 · Mirage Quattro Full Face Mask · Resmed, Ltd. · 2007K113127 · Mirage Quattro · Resmed, Ltd. · 201219801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 3 other ancestors3 generations back: 5 other ancestors4 generations back: 5 other ancestors5 generations back: 1 other ancestor 1 generation forward: 1 descendant K113127 · Mirage Quattro · Resmed, Ltd. · 2012K063122 · Mirage Quattro Full Face Mask · Resmed, Ltd. · 2007K042403 · Mirage Swift · Resmed, Ltd. · 2004K032916 · Mirage Activa Mask · Resmed, Ltd. · 2003K023244 · Mirage Full Face Mask Series 2 · Resmed, Ltd. · 2002K982530 · Sullivan Mirage Full Face Mask · Resmed, Ltd. · 1998−50
  1. Root · 6 generations backK982530 Sullivan Mirage Full Face MaskResmed, Ltd. · 1998
  2. 5 generations backK023244 Mirage Full Face Mask Series 2Resmed, Ltd. · 2002
  3. 4 generations backK032916 Mirage Activa MaskResmed, Ltd. · 2003
  4. 3 generations backK042403 Mirage SwiftResmed, Ltd. · 2004
  5. 2 generations backK063122 Mirage Quattro Full Face MaskResmed, Ltd. · 2007
  6. 1 generation backK113127 Mirage QuattroResmed, Ltd. · 2012
  7. This deviceK133009 Nasal Mask, Nasal Mask, Full Face MaskBMC Medical Co., Ltd. · 2014
  8. Descendant · cites it directly · 0 of its ownK163464 Viva Nasal Mask (Model: NM4), Numa Full Face Mask (Model: BMC-FM2)Bmc Medical., Ltd. · 2017

Most influential descendants

Showing 1 of 1 · See all
  • K163464Viva Nasal Mask (Model: NM4), Numa Full Face Mask (Model: BMC-FM2)Bmc Medical., Ltd. · 2017 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K982530Sullivan Mirage Full Face MaskResmed, Ltd.1998—
−5K023244Mirage Full Face Mask Series 2Resmed, Ltd.2002—
−4K032916Mirage Activa MaskResmed, Ltd.2003—
−3K042403Mirage SwiftResmed, Ltd.2004—
−2K063122Mirage Quattro Full Face MaskResmed, Ltd.2007—
−1K113127Mirage QuattroResmed, Ltd.2012—
0 (this device)K133009Nasal Mask, Nasal Mask, Full Face MaskBMC Medical Co., Ltd.2014—
+1K163464Viva Nasal Mask (Model: NM4), Numa Full Face Mask (Model: BMC-FM2)Bmc Medical., Ltd.2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198310
198810
199010
199630
199810
199920
200010
200220
200320
200810
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
FIG. 1 — Lineage of K133009, 1998–2017Source: 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? (3)

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
*K092835Comfortgel Nasal Mask
Summary page 1
…Number: 2I1CFR 868.5905 Device Class: 11 3. Predicate Device 3.1 Predicate Device of Nasal Mask BMC-NM and BMC-NM2 Product name: ComfortoerM (K092835) Manufacturer: RESPIRONICS Product name: Mirage Activa m(K030798) Manufacturer: Resme…
Respironics Inc., Sleep & Home Respiratory Group2010—
*K030798Mirage Activa Mask
Summary page 1
…evice of Nasal Mask BMC-NM and BMC-NM2 Product name: ComfortoerM (K092835) Manufacturer: RESPIRONICS Product name: Mirage Activa m(K030798) Manufacturer: Resmed Product Code: BZD Intended Use: * Mirage ActivaTM Mask (K030798): Mirage Ac…
Resmed, Ltd.2003—
*K113127Mirage QuattroResmed, Ltd.2012—

Also cleared against K092835: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K163464Viva Nasal Mask (Model: NM4), Numa Full Face Mask (Model: BMC-FM2)Bmc Medical., Ltd.20170

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 2 companies; a new generation was cleared every 2.3 years on median.
  • 1 of the 22 ancestors has a recall of any class.
  • Of its descendants, K163464 (Bmc Medical., Ltd., 2017) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K092835.

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. 2014, 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 BMC-NM, BMC-NM2 Nasal Mask and BMC-FM full face mask channel airflow noninvasively to a patient from a positive airway pressure device such as a continuous positive airway pressure (CPAP) or Bi-level system.

The BMC-NM, BMC-NM2 Nasal Mask and BMC-FM full face mask are:

* To be used by adult patients (>661bs / >30kg) for whom positive airway pressure has been prescribed.

Intended for single-patient reuse in home environment and multi-patient re-use in the hospital/institutional 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. “K133009: Nasal Mask, Nasal Mask, Full Face Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K133009

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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