510(k) · Cleared
ClearedSullivan Mirage 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 Oct 16, 1998 after an 88-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 12 of the 133 devices in its family, counting itself, have a Class I recall. 132 later devices descend from it.
- Decided
- Oct 16, 1998
- Review
- 88 days
- Class
- Class II
- Product code
- BZD
- Recalls
- None
- Predicates
- 0
132 later devices descend from it, 7 citing it directly. 12 of the 133 devices in this family, counting this one, have a Class I recall.
- This deviceK982530 Sullivan Mirage Full Face MaskResmed, Ltd. · 1998
- Descendant · cites it directly · 113 of its ownK023244 Mirage Full Face Mask Series 2Resmed, Ltd. · 2002
- Descendant · cites it directly · 96 of its ownK023306 Mirage Full Face Mask Series 2Resmed, Ltd. · 2002
- Descendant · cites it directly · 96 of its ownK023284 Mirage Full Face Mask Series 2Resmed, Ltd. · 2002
- Descendant · 2 generations on · 93 of its ownK032916 Mirage Activa MaskResmed, Ltd. · 2003
- Descendant · 2 generations on · 80 of its ownK042403 Mirage SwiftResmed, Ltd. · 2004
Showing 5 of 132 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
Most influential descendants
Showing 5 of 132 · See all- K023244Mirage Full Face Mask Series 2Resmed, Ltd. · 2002 · cites it directly113descendants
- K023306Mirage Full Face Mask Series 2Resmed, Ltd. · 2002 · cites it directly96descendants
- K023284Mirage Full Face Mask Series 2Resmed, Ltd. · 2002 · cites it directly96descendants
- K032916Mirage Activa MaskResmed, Ltd. · 2003 · 2 generations on93descendants
- K042403Mirage SwiftResmed, Ltd. · 2004 · 2 generations on80descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K982530 | Sullivan Mirage Full Face Mask | Resmed, Ltd. | 1998 | — |
| +1 | K023244 | Mirage Full Face Mask Series 2 | Resmed, Ltd. | 2002 | — |
| +1 | K023306 | Mirage Full Face Mask Series 2 | Resmed, Ltd. | 2002 | — |
| +1 | K023284 | Mirage Full Face Mask Series 2 | Resmed, Ltd. | 2002 | — |
| +2 | K032916 | Mirage Activa Mask | Resmed, Ltd. | 2003 | — |
| +2 | K042403 | Mirage Swift | Resmed, Ltd. | 2004 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 4 | 0 |
| 2003 | 4 | 0 |
| 2004 | 5 | 0 |
| 2005 | 5 | 0 |
| 2006 | 7 | 0 |
| 2007 | 6 | 1 |
| 2008 | 8 | 1 |
| 2009 | 9 | 0 |
| 2010 | 3 | 0 |
| 2011 | 9 | 0 |
| 2012 | 10 | 1 |
| 2013 | 12 | 1 |
| 2014 | 3 | 0 |
| 2015 | 4 | 1 |
| 2016 | 4 | 2 |
| 2017 | 5 | 1 |
| 2018 | 4 | 1 |
| 2019 | 4 | 3 |
| 2020 | 3 | 0 |
| 2021 | 4 | 0 |
| 2022 | 1 | 0 |
| 2023 | 4 | 0 |
| 2024 | 6 | 0 |
| 2025 | 3 | 0 |
| 2026 | 5 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
12 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?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (132)
See all 1327 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K023244 | Mirage Full Face Mask Series 2 | 2002 | 113 |
| K023306 | Mirage Full Face Mask Series 2 | 2002 | 96 |
| K023284 | Mirage Full Face Mask Series 2 | 2002 | 96 |
| K020759 | 7600 Series Reusable Full-Face Cpap/Nippv Masks Models 7620 Large, 7630 Medium, 7640… | 2002 | 26 |
| K022642 | Twlight, Model Isp 9600 | 2003 | 2 |
| K033914 | Oxygen Diverter Valve | 2004 | 0 |
| K023683 | Multi-Strap Full Face Mask | 2003 | 0 |
Has anything in its family been recalled? (12 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.
- K183512Moore Park MaskResmed, Ltd. · 2019 · 3 generations on · ◆ in the 2019 descendants bar of FIG. 11 Class I recall
- K120463Mojo, VerasealSleepnet Corporation · 2012 · 3 generations on · ◆ in the 2012 descendants bar of FIG. 11 Class I recall
- K153563AirFit F20Resmed, Ltd. · 2016 · 3 generations on · ◆ in the 2016 descendants bar of FIG. 11 Class I recall
- K132887Airfit N10Resmed, Ltd. · 2013 · 4 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
- K063806Sleepnet Mojo -NV Full Face Mask, Non-VentedSleepnet Corporation · 2007 · 4 generations on · ◆ in the 2007 descendants bar of FIG. 11 Class I recall
- K081743Classicstar NV SE and Novastar NV SE and Aav Full Face MasksDraeger Medical AG & Co. KG · 2008 · 4 generations on · ◆ in the 2008 descendants bar of FIG. 12 Class I recalls
- K190254Mojo 2 Full Face Vented Mask, Veraseal 3 Full Face Vented Mask, V3 Full Face Vented MaskSleepnet Corporation · 2019 · 4 generations on · ◆ in the 2019 descendants bar of FIG. 11 Class I recall
- K170924AirFit F20Resmed, Ltd. · 2018 · 4 generations on · ◆ in the 2018 descendants bar of FIG. 12 Class I recalls
- K190533Mojo 2 Full Face Non-Vented Mask, Mojo 2 AAV Non-Vented Full-Face Mask, Veraseal 3 Full Face Non-Vented…Sleepnet Corporation · 2019 · 5 generations on · ◆ in the 2019 descendants bar of FIG. 12 Class I recalls
- K140980TI Nasal MaskRespironics, Inc. · 2015 · 6 generations on · ◆ in the 2015 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 12; all are on the web page.
What does this lineage say?
- Of its descendants, K023244 (Resmed, Ltd., 2002) has gone furthest, with 113 descendants of its own.
How does its category compare?
All BZD devicesBZD Ventilator, Non-Continuous (Respirator): FDA decisions, review times, recalls and adverse event reports over 20 years.
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 Sullivan® Mirage™ Full Face Mask is a patient interface accessory for use with Constant Positive Airway Pressure (CPAP) and bilevel systems used in the treatment of adult Obstructive Sleep Apnea (OSA) and/or ventilatory support.
Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K982530 · printed Nov 4, 2026
Cite this page
510(k) Report. “K982530: Sullivan Mirage Full Face Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K982530
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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