510(k) · Cleared
ClearedF6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
BMC Medical Co., Ltd. · BZD Ventilator, Non-Continuous (Respirator)
Cleared on Apr 29, 2026 as substantially equivalent to K210844 (Respironics, Inc., 2021) and 1 other predicate after a 215-day review. Its family tree reaches back 9 generations to 1996. 3 of the 39 devices in its family, counting itself, have a Class I recall.
- Decided
- Apr 29, 2026
- Review
- 215 days
- Class
- Class II
- Product code
- BZD
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 9 generations to K945938 (1996). 38 ancestors in all, the oldest K833786 (1983). No later device cites it as a predicate yet. 3 of the 39 devices in this family, counting this one, have a Class I recall.
- Root · 9 generations backK945938 Respironics Monarch Mini MaskRespironics, Inc. · 1996
- 5 generations between
- 3 generations backK121631 Simple T Nasal MaskRespironics, Inc. · 2012 · Recalled (Class I)
- 2 generations backK140980 TI Nasal MaskRespironics, Inc. · 2015 · Recalled (Class I)
- 1 generation backK210844 DreamWear Silicone Pillows MaskRespironics, Inc. · 2021
- This deviceK253166 F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)BMC Medical Co., Ltd. · 2026
Show all 9 generations
- Root · 9 generations backK945938 Respironics Monarch Mini MaskRespironics, Inc. · 1996
- 8 generations backK992336 Monarch II Mini MaskRespironics, Inc. · 1999
- 7 generations backK053352 Comfortlite Nasal MaskRespironics, Inc. · 2006
- 6 generations backK082558 Comfortlite Nasal MaskRespironics, Inc. · 2009
- 5 generations backK102502 Golife Nasal MaskRespironics, Inc. · 2010
- 4 generations backK110008 Golife Nasal MaskRespironics, Inc. · 2011
- 3 generations backK121631 Simple T Nasal MaskRespironics, Inc. · 2012 · Recalled (Class I)
- 2 generations backK140980 TI Nasal MaskRespironics, Inc. · 2015 · Recalled (Class I)
- 1 generation backK210844 DreamWear Silicone Pillows MaskRespironics, Inc. · 2021
- This deviceK253166 F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)BMC Medical Co., Ltd. · 2026
Class I recalls in this family
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K945938 | Respironics Monarch Mini Mask | Respironics, Inc. | 1996 | — |
| −8 | K992336 | Monarch II Mini Mask | Respironics, Inc. | 1999 | — |
| −7 | K053352 | Comfortlite Nasal Mask | Respironics, Inc. | 2006 | — |
| −6 | K082558 | Comfortlite Nasal Mask | Respironics, Inc. | 2009 | — |
| −5 | K102502 | Golife Nasal Mask | Respironics, Inc. | 2010 | — |
| −4 | K110008 | Golife Nasal Mask | Respironics, Inc. | 2011 | — |
| −3 | K121631 | Simple T Nasal Mask | Respironics, Inc. | 2012 | Class I |
| −2 | K140980 | TI Nasal Mask | Respironics, Inc. | 2015 | Class I |
| −1 | K210844 | DreamWear Silicone Pillows Mask | Respironics, Inc. | 2021 | — |
| 0 (this device) | K253166 | F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S) | BMC Medical Co., Ltd. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1983 | 1 | 0 |
| 1988 | 1 | 0 |
| 1990 | 1 | 0 |
| 1996 | 3 | 0 |
| 1998 | 3 | 0 |
| 1999 | 2 | 0 |
| 2000 | 1 | 0 |
| 2002 | 3 | 0 |
| 2003 | 4 | 0 |
| 2004 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
| 2009 | 1 | 0 |
| 2010 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 1 | 0 |
| 2013 | 1 | 0 |
| 2019 | 1 | 1 |
| 2024 | 1 | 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.
3 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K210844 | DreamWear Silicone Pillows MaskSummary page 5…Ventilator, Non-Continuous (Respirator) Product Code: BZD Predicate Device: DreamWear Silicone Pillows Mask - K210844 Common/Usual Name: CPAP Mask Classification Name: Ventilator, Non-Continuous (Respirator) Pro… | 2021 |
| * | K234134 | AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask SystemSummary page 5…: Ventilator, Non-Continuous (Respirator) Product Code: BZD Predicate Device: AirFit F30i NM Mask System - K234134 Common/Usual Name: CPAP Mask Classification Name: Ventilator, Non-Continuous (Respirator) Pro… | 2024 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (3 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 · 2 generations back · ◆ in the 2019 ancestors bar of FIG. 11 Class I recall
- K140980TI Nasal MaskRespironics, Inc. · 2015 · 2 generations back · ◆ on the line of descent in FIG. 11 Class I recall
- K121631Simple T Nasal MaskRespironics, Inc. · 2012 · 3 generations back · ◆ on the line of descent in FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 30 years and passes through 2 companies; a new generation was cleared every 3.1 years on median.
- 4 of the 38 ancestors have a recall of any class; 3 have a Class I recall.
How does its category compare?
All BZD devicesBZD Ventilator, Non-Continuous (Respirator): FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, 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 Nasal Pillows Interface (P6S) is intended to provide an interface for patients who have been prescribed CPAP or bi-level therapy. The Nasal Pillows Interface (P6S) is:
- to be used by patients (> 66 lbs. / 30 kg) for whom positive airway pressure therapy has been prescribed.
- intended for single-patient re-use in the home environment.
The Full Face Mask (F6S) is intended to provide an interface for patients who have been prescribed CPAP or bi-level therapy. The Full Face Mask (F6S) is:
- to be used by patients (> 66 lbs. / 30 kg) for whom positive airway pressure therapy has been prescribed.
- intended for single-patient re-use in the home environment.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K253166 · printed Nov 6, 2026
Cite this page
510(k) Report. “K253166: F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K253166
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Record history
- FDA decision record loaded Oct 30, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026