510(k) · Cleared
Cleared3B Resmart Cpap and Auto Cpap Systems, BMC Resmart Cpap and Auto Cpap Systems
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
3B Medical, Inc. · BZD Ventilator, Non-Continuous (Respirator)
Cleared on Aug 22, 2013 as substantially equivalent to K110629 (3B Products, Inc., 2012) after a 72-day review. Its family tree reaches back 4 generations to 1996. 4 later devices descend from it.
- Decided
- Aug 22, 2013
- Review
- 72 days
- Class
- Class II
- Product code
- BZD
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K953930 (1996). 11 ancestors in all. 4 later devices descend from it, 1 citing it directly.
- Root · 4 generations backK953930 Virtuoso Smart Cpap SystemRespironics, Inc. · 1996
- 3 generations backK993433 Virtuoso LX Smart Cpap SystemRespironics, Inc. · 1999
- 2 generations backK012554 Remstar Auto Cpap SystemRespironics, Inc. · 2002
- 1 generation backK110629 Resmart Cpap, Resmart Auto-Cpap and Resmart Humidifier3B Products, Inc. · 2012
- This deviceK131707 3B Resmart Cpap and Auto Cpap Systems, BMC Resmart Cpap and Auto…3B Medical, Inc. · 2013
- Descendant · cites it directly · 3 of its ownK133769 3B Resmart Bpap 25A, BMC Resmart Bpap 25A3B Medical, Inc. · 2014
- Descendant · 2 generations on · 2 of its ownK201620 Luna® G3 BPAP 25A3B Medical, Inc. · 2021
- Descendant · 3 generations on · 0 of its ownK213169 BPAP SystemBMC Medical Co., Ltd. · 2022
- Descendant · 3 generations on · 0 of its ownK212263 Luna G3 BPAP System3B Medical, Inc. · 2022
Most influential descendants
Showing 4 of 4 · See all- K1337693B Resmart Bpap 25A, BMC Resmart Bpap 25A3B Medical, Inc. · 2014 · cites it directly3descendants
- K201620Luna® G3 BPAP 25A3B Medical, Inc. · 2021 · 2 generations on2descendants
- K213169BPAP SystemBMC Medical Co., Ltd. · 2022 · 3 generations on0descendants
- K212263Luna G3 BPAP System3B Medical, Inc. · 2022 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K953930 | Virtuoso Smart Cpap System | Respironics, Inc. | 1996 | — |
| −3 | K993433 | Virtuoso LX Smart Cpap System | Respironics, Inc. | 1999 | — |
| −2 | K012554 | Remstar Auto Cpap System | Respironics, Inc. | 2002 | — |
| −1 | K110629 | Resmart Cpap, Resmart Auto-Cpap and Resmart Humidifier | 3B Products, Inc. | 2012 | — |
| 0 (this device) | K131707 | 3B Resmart Cpap and Auto Cpap Systems, BMC Resmart Cpap and Auto Cpap Systems | 3B Medical, Inc. | 2013 | — |
| +1 | K133769 | 3B Resmart Bpap 25A, BMC Resmart Bpap 25A | 3B Medical, Inc. | 2014 | — |
| +2 | K201620 | Luna® G3 BPAP 25A | 3B Medical, Inc. | 2021 | — |
| +3 | K213169 | BPAP System | BMC Medical Co., Ltd. | 2022 | — |
| +3 | K212263 | Luna G3 BPAP System | 3B Medical, Inc. | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 1998 | 2 | 0 |
| 2001 | 1 | 0 |
| 2002 | 2 | 0 |
| 2003 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 2 | 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.
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 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? (1)
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 |
|---|---|---|---|
| * | K110629 | Resmart Cpap, Resmart Auto-Cpap and Resmart HumidifierSummary page 1…BZO -Non-continuous Ventilator (Respirator) Medical Specialties Anesthesiology Predicate Device(s) RESmart CPAP and Auto CPAP System (K110629) Section 7 510(k) Summary (K(131707) RESmart CPAP/Auto CPAP Intended Use… | 2012 |
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K133769 | 3B Resmart Bpap 25A, BMC Resmart Bpap 25A | 2014 | 3 |
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 17 years and passes through 3 companies; a new generation was cleared every 3.1 years on median.
- 1 of the 11 ancestors has a recall of any class.
- Of its descendants, K133769 (3B Medical, Inc., 2014) has gone furthest, with 3 descendants of its own.
- 1 other device also cites its predicate K110629.
How does its category compare?
All BZD devicesBZD Ventilator, Non-Continuous (Respirator): FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, 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 3B and BMVC RESmart CPAP and Auto CPAP Systems are intended to deliver positive pressure for the treatment of Obstructive Sleep Apnea. The optional integrated humidifier is indicated for the humidification and warming of air from the flow generator device. These devices are intended far single patient use by prescription in the home or hospital/intuitional environment on adult patients.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K131707 · printed Nov 5, 2026
Cite this page
510(k) Report. “K131707: 3B Resmart Cpap and Auto Cpap Systems, BMC Resmart Cpap and Auto Cpap Systems.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K131707
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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