510(k) · Cleared
ClearedMirage Quattro Full Face Mask
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Resmed, Ltd. · BZD Ventilator, Non-Continuous (Respirator)
Cleared on Feb 2, 2007 as substantially equivalent to K023244 (Resmed, Ltd., 2002) and 3 other predicates after a 113-day review. Its family tree reaches back 4 generations to 1998. 7 of the 51 devices in its family, counting itself, have a Class I recall. 38 later devices descend from it.
- Decided
- Feb 2, 2007
- Review
- 113 days
- Class
- Class II
- Product code
- BZD
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 4 generations to K982530 (1998). 12 ancestors in all, the oldest K900164 (1990). 38 later devices descend from it, 7 citing it directly. 7 of the 51 devices in this family, counting this one, have a Class I recall.
- Root · 4 generations backK982530 Sullivan Mirage Full Face MaskResmed, Ltd. · 1998
- 3 generations backK023244 Mirage Full Face Mask Series 2Resmed, Ltd. · 2002
- 2 generations backK032916 Mirage Activa MaskResmed, Ltd. · 2003
- 1 generation backK042403 Mirage SwiftResmed, Ltd. · 2004
- This deviceK063122 Mirage Quattro Full Face MaskResmed, Ltd. · 2007
- Descendant · cites it directly · 26 of its ownK072940 Mirage MicroResmed, Ltd. · 2007
- Descendant · 2 generations on · 19 of its ownK102746 Mirage FXResmed, Ltd. · 2010
- Descendant · cites it directly · 9 of its ownK123979 Quattro AirResmed, Ltd. · 2013 · Recalled
- Descendant · 3 generations on · 8 of its ownK123789 Swift FX NanoResmed, Ltd. · 2013
- Descendant · 4 generations on · 7 of its ownK132887 Airfit N10Resmed, Ltd. · 2013 · Recalled (Class I)
Showing 5 of 38 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
Most influential descendants
Showing 5 of 38 · See all- K072940Mirage MicroResmed, Ltd. · 2007 · cites it directly26descendants
- K102746Mirage FXResmed, Ltd. · 2010 · 2 generations on19descendants
- K123979Quattro AirResmed, Ltd. · 2013 · cites it directly9descendants
- K123789Swift FX NanoResmed, Ltd. · 2013 · 3 generations on8descendants
- K132887Airfit N10Resmed, Ltd. · 2013 · 4 generations on7descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K982530 | Sullivan Mirage Full Face Mask | Resmed, Ltd. | 1998 | — |
| −3 | K023244 | Mirage Full Face Mask Series 2 | Resmed, Ltd. | 2002 | — |
| −2 | K032916 | Mirage Activa Mask | Resmed, Ltd. | 2003 | — |
| −1 | K042403 | Mirage Swift | Resmed, Ltd. | 2004 | — |
| 0 (this device) | K063122 | Mirage Quattro Full Face Mask | Resmed, Ltd. | 2007 | — |
| +1 | K072940 | Mirage Micro | Resmed, Ltd. | 2007 | — |
| +2 | K102746 | Mirage FX | Resmed, Ltd. | 2010 | — |
| +1 | K123979 | Quattro Air | Resmed, Ltd. | 2013 | 1 |
| +3 | K123789 | Swift FX Nano | Resmed, Ltd. | 2013 | — |
| +4 | K132887 | Airfit N10 | Resmed, Ltd. | 2013 | Class I |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1990 | 1 | 0 |
| 1996 | 1 | 0 |
| 1998 | 1 | 0 |
| 1999 | 1 | 0 |
| 2002 | 2 | 0 |
| 2003 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 1 | 0 |
| 2008 | 2 | 0 |
| 2009 | 2 | 0 |
| 2010 | 3 | 0 |
| 2011 | 2 | 0 |
| 2012 | 2 | 1 |
| 2013 | 5 | 1 |
| 2014 | 2 | 0 |
| 2015 | 2 | 0 |
| 2016 | 3 | 2 |
| 2017 | 2 | 1 |
| 2018 | 2 | 1 |
| 2019 | 1 | 1 |
| 2021 | 1 | 0 |
| 2023 | 2 | 0 |
| 2024 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 3 | 0 |
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.
7 devices in this family have a Class I recall. 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 K250624 myAirscore 15.7 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K023244 | Mirage Full Face Mask Series 2Summary page 1…Accessory to Noncontinuous Ventilator (IPPB) Classification 21 CFR 868.5905, 73 BZD (Class 11) Predicate Device Mirage FFM Series 2 (K023244, K023284 and K023306), Mirage Swift (K042403). Description The Mirage Qu… | 2002 |
| * | K023284 | Mirage Full Face Mask Series 2Summary page 1…to Noncontinuous Ventilator (IPPB) Classification 21 CFR 868.5905, 73 BZD (Class 11) Predicate Device Mirage FFM Series 2 (K023244, K023284 and K023306), Mirage Swift (K042403). Description The Mirage Quattro FFM… | 2002 |
| * | K023306 | Mirage Full Face Mask Series 2Summary page 1…nuous Ventilator (IPPB) Classification 21 CFR 868.5905, 73 BZD (Class 11) Predicate Device Mirage FFM Series 2 (K023244, K023284 and K023306), Mirage Swift (K042403). Description The Mirage Quattro FFM provides se… | 2002 |
| * | K042403 | Mirage SwiftSummary page 1…on 21 CFR 868.5905, 73 BZD (Class 11) Predicate Device Mirage FFM Series 2 (K023244, K023284 and K023306), Mirage Swift (K042403). Description The Mirage Quattro FFM provides seal such that air flow… | 2004 |
What descends from it? (38)
See all 387 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (7 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K120463Mojo, VerasealSleepnet Corporation · 2012 · Cites it directly · ◆ in the 2012 descendants bar of FIG. 11 Class I recall
- K190254Mojo 2 Full Face Vented Mask, Veraseal 3 Full Face Vented Mask, V3 Full Face Vented MaskSleepnet Corporation · 2019 · 2 generations on · ◆ in the 2019 descendants bar of FIG. 11 Class I recall
- K153563AirFit F20Resmed, Ltd. · 2016 · 2 generations on · ◆ in the 2016 descendants bar of FIG. 11 Class I recall
- K170924AirFit F20Resmed, Ltd. · 2018 · 3 generations on · ◆ in the 2018 descendants bar of FIG. 12 Class I recalls
- K132887Airfit N10Resmed, Ltd. · 2013 · 4 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
- K161978AirFit N20Resmed, Ltd. · 2016 · 6 generations on · ◆ in the 2016 descendants bar of FIG. 11 Class I recall
- K171212AirFit N20Resmed, Ltd. · 2017 · 7 generations on · ◆ in the 2017 descendants bar of FIG. 11 Class I recall
Nearest 5 of 7; all are on the web page.
What does this lineage say?
- The line of descent spans 9 years and passes through 1 company; a new generation was cleared every 2.3 years on median.
- None of the 12 ancestors has a recall.
- Of its descendants, K072940 (Resmed, Ltd., 2007) has gone furthest, with 26 descendants of its own.
- 11 other devices also cite its predicate K023244.
How does its category compare?
All BZD devicesBZD Ventilator, Non-Continuous (Respirator): FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · BZD
7in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · BZD
189in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · BZD
8in 2023
Class I (13 since 2007) Class II/III not classified
Adverse event reports per year · BZD
60,279in 2025
MAUDE reports naming product code BZD, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 21 | 83 | 29 | 65 |
| 2008 | 17 | 108 | 2 | 67 |
| 2009 | 23 | 90 | 1 | 147 |
| 2010 | 12 | 122 | 0 | 143 |
| 2011 | 23 | 125 | 1 | 189 |
| 2012 | 21 | 133 | 0 | 139 |
| 2013 | 23 | 127 | 0 | 82 |
| 2014 | 14 | 172 | 0 | 86 |
| 2015 | 11 | 224 | 0 | 114 |
| 2016 | 12 | 217 | 0 | 118 |
| 2017 | 5 | 221 | 0 | 148 |
| 2018 | 5 | 280 | 0 | 101 |
| 2019 | 6 | 231 | 4 (4) | 188 |
| 2020 | 6 | 137 | 0 | 126 |
| 2021 | 6 | 192 | 0 | 6,066 |
| 2022 | 4 | 253 | 0 | 90,768 |
| 2023 | 5 | 204 | 8 (7) | 27,987 |
| 2024 | 10 | 132 | 0 | 68,262 |
| 2025 | 7 | 189 | 0 | 60,279 |
| 2026 | 10 | 214 | 2 (2) | — |
What is it indicated for?
The Mirage Quattro channels airflow noninvasively to a patient from a positive airway pressure device such as a continuous positive airway pressure (CPAP) or bilevel system.
The Mirage Quattro is to be used by adult patients (>661b / >30kg) for whom positive airway pressure has been prescribed.
The Mirage Quattro FFM intended for single patient re-use in the home environment and/or multi-patient reuse in the hospital/institutional environment.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K063122 · printed Nov 5, 2026
Cite this page
510(k) Report. “K063122: Mirage Quattro 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/K063122
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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