510(k) Report

510(k) · Cleared

Cleared

Viva Nasal Mask (Model: NM4), Numa Full Face Mask (Model: BMC-FM2)

K163464510(k) TraditionalCleared Sep 5, 2017270-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., Ltd. · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Sep 5, 2017 as substantially equivalent to K133009 (BMC Medical Co., Ltd., 2014) and 1 other predicate after a 270-day review. Its family tree reaches back 8 generations to 1998.

Decided
Sep 5, 2017
Review
270 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K982530 (1998). 34 ancestors in all, the oldest K833786 (1983). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2014: 1 other ancestor2012: 1 other ancestor2010: 1 other ancestor2003: 2 other ancestors2009: 1 other ancestor2008: 1 other ancestor2005: 2 other ancestors2002: 2 other ancestors1999: 3 other ancestors1996: 4 other ancestors2007: 1 other ancestor2006: 1 other ancestor2000: 1 other ancestor1998: 2 other ancestors1990: 1 other ancestor1988: 1 other ancestor1983: 1 other ancestorReference device: K112277 · BD Veritor (TM) System for Rapid Detection of Flu a+B · Becton, Dickinson and Company · 2011 · recalledK982530 · 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. · 2007K072940 · Mirage Micro · Resmed, Ltd. · 2007K102746 · Mirage FX · Resmed, Ltd. · 2010K123979 · Quattro Air · Resmed, Ltd. · 2013 · recalled1980199020002010
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 8 other ancestors4 generations back: 7 other ancestors5 generations back: 6 other ancestors6 generations back: 1 other ancestor K123979 · Quattro Air · Resmed, Ltd. · 2013 · recalledK102746 · Mirage FX · Resmed, Ltd. · 2010K072940 · Mirage Micro · Resmed, Ltd. · 2007K063122 · 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 · 8 generations backK982530 Sullivan Mirage Full Face MaskResmed, Ltd. · 1998
  2. 7 generations backK023244 Mirage Full Face Mask Series 2Resmed, Ltd. · 2002
  3. 6 generations backK032916 Mirage Activa MaskResmed, Ltd. · 2003
  4. 5 generations backK042403 Mirage SwiftResmed, Ltd. · 2004
  5. 4 generations backK063122 Mirage Quattro Full Face MaskResmed, Ltd. · 2007
  6. 3 generations backK072940 Mirage MicroResmed, Ltd. · 2007
  7. 2 generations backK102746 Mirage FXResmed, Ltd. · 2010
  8. 1 generation backK123979 Quattro AirResmed, Ltd. · 2013 · Recalled
  9. This deviceK163464 Viva Nasal Mask (Model: NM4), Numa Full Face Mask (Model: BMC-FM2)Bmc Medical., Ltd. · 2017
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K982530Sullivan Mirage Full Face MaskResmed, Ltd.1998—
−7K023244Mirage Full Face Mask Series 2Resmed, Ltd.2002—
−6K032916Mirage Activa MaskResmed, Ltd.2003—
−5K042403Mirage SwiftResmed, Ltd.2004—
−4K063122Mirage Quattro Full Face MaskResmed, Ltd.2007—
−3K072940Mirage MicroResmed, Ltd.2007—
−2K102746Mirage FXResmed, Ltd.2010—
−1K123979Quattro AirResmed, Ltd.20131
0 (this device)K163464Viva 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
199640
199820
199930
200010
200220
200320
200520
200610
200710
200810
200910
201010
201210
201410
FIG. 1 — Lineage of K163464, 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? (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
*K133009Nasal Mask, Nasal Mask, Full Face Mask
Summary page 4
…Device Class: II Predicate Device(s) Predicate Device of Viva Nasal Mask: BMC-NM2 Nasal Mask (K133009) Predicate Device of Numa Full Face Mask: Quattro™ Air (K123979)…
BMC Medical Co., Ltd.2014—
*K123979Quattro Air
Summary page 4
…al Mask (K133009) Predicate Device of Numa Full Face Mask: Quattro™ Air (K123979) 1 Reference Devic…
Resmed, Ltd.20131
†K112277BD Veritor (TM) System for Rapid Detection of Flu a+BBecton, Dickinson and Company20111

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 2 companies; a new generation was cleared every 2.3 years on median.
  • 2 of the 34 ancestors have a recall of any class.

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. 2017, 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 Viva Nasal Mask channels airflow noninvasively to a patient from a positive airway pressure device such as a continuous positive airway pressure (CPAP) or bi-level system.

The Viva Nasal Mask is:

To be used by adult patients (>66lbs / >30kg) for whom positive airway pressure has been prescribed.

Intended for single-patient reuse.

The Numa Full Face Mask channels airflow noninvasively to a patient from a positive airway pressure device such as a continuous positive airway pressure (CPAP) or Bi-level system.

The Numa Full Face Mask is:

To be used by adult patients (>66lbs / >30kg) for whom positive airway pressure has been prescribed.

Intended for single-patient reuse.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K163464: Viva Nasal Mask (Model: NM4), Numa Full Face Mask (Model: BMC-FM2).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K163464

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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