510(k) · Cleared
ClearedAdjustable Peep Valve
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Vital Signs, Inc. · BYE Attachment, Breathing, Positive End Expiratory Pressure
Cleared on Jan 8, 1991 after a 70-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 of the 6 devices in its family, counting itself, has a Class I recall. 5 later devices descend from it.
- Decided
- Jan 8, 1991
- Review
- 70 days
- Class
- Class II
- Product code
- BYE
- Recalls
- None
- Predicates
- 0
5 later devices descend from it, 1 citing it directly. 1 of the 6 devices in this family, counting this one, has a Class I recall.
- This deviceK904874 Adjustable Peep ValveVital Signs, Inc. · 1991
- Descendant · cites it directly · 4 of its ownK013884 Boussignac C.P.a.P. DeviceVygon SA · 2003
- Descendant · 2 generations on · 0 of its ownK123957 Pneupac Parapac PlusSmiths Medical International, Ltd. · 2013 · Recalled (Class I)
- Descendant · 2 generations on · 0 of its ownK122610 Plaxtron Cpap System, Model CH-FFM-87XX/CH-FFM-88XX SeriesSen MU Technology Co., Ltd. · 2013
- Descendant · 2 generations on · 0 of its ownK112546 O_Two Cpap SystemO-Two Medical Technologies, Inc. · 2011
- Descendant · 2 generations on · 0 of its ownK090710 Mercury CpapMercury Medical · 2009
Class I recalls in this family
- K123957 Pneupac Parapac Plus2 generations on · 2013
Most influential descendants
Showing 5 of 5 · See all- K013884Boussignac C.P.a.P. DeviceVygon SA · 2003 · cites it directly4descendants
- K123957Pneupac Parapac PlusSmiths Medical International, Ltd. · 2013 · 2 generations on0descendants
- K122610Plaxtron Cpap System, Model CH-FFM-87XX/CH-FFM-88XX SeriesSen MU Technology Co., Ltd. · 2013 · 2 generations on0descendants
- K112546O_Two Cpap SystemO-Two Medical Technologies, Inc. · 2011 · 2 generations on0descendants
- K090710Mercury CpapMercury Medical · 2009 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K904874 | Adjustable Peep Valve | Vital Signs, Inc. | 1991 | — |
| +1 | K013884 | Boussignac C.P.a.P. Device | Vygon SA | 2003 | — |
| +2 | K123957 | Pneupac Parapac Plus | Smiths Medical International, Ltd. | 2013 | Class I |
| +2 | K122610 | Plaxtron Cpap System, Model CH-FFM-87XX/CH-FFM-88XX Series | Sen MU Technology Co., Ltd. | 2013 | — |
| +2 | K112546 | O_Two Cpap System | O-Two Medical Technologies, Inc. | 2011 | — |
| +2 | K090710 | Mercury Cpap | Mercury Medical | 2009 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2003 | 1 | 0 |
| 2009 | 1 | 0 |
| 2011 | 1 | 0 |
| 2013 | 2 | 1 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
1 device in this family has a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K013884 | Boussignac C.P.a.P. Device | 2003 | 4 |
Has anything in its family been recalled? (1 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.
- K123957Pneupac Parapac PlusSmiths Medical International, Ltd. · 2013 · 2 generations on · ◆ in the 2013 descendants bar of FIG. 16 Class I recalls
What does this lineage say?
- Of its descendants, K013884 (Vygon SA, 2003) has gone furthest, with 4 descendants of its own.
How does its category compare?
All BYE devicesBYE Attachment, Breathing, Positive End Expiratory Pressure: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · BYE
1in 2016
2026 to Oct 25, outlined.
Median 510(k) review, days · BYE
117in 2011
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · BYE
1in 2015
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · BYE
7in 2025
MAUDE reports naming product code BYE, 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 | 1 | — | 4 | 8 |
| 2008 | 1 | — | 2 | 3 |
| 2009 | 3 | 155 | 0 | 1 |
| 2010 | 1 | — | 0 | 4 |
| 2011 | 3 | 117 | 0 | 2 |
| 2012 | 0 | — | 0 | 6 |
| 2013 | 1 | — | 0 | 2 |
| 2014 | 2 | — | 0 | 8 |
| 2015 | 0 | — | 1 | 4 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 3 |
| 2018 | 0 | — | 0 | 11 |
| 2019 | 0 | — | 0 | 5 |
| 2020 | 0 | — | 0 | 5 |
| 2021 | 0 | — | 0 | 4 |
| 2022 | 0 | — | 0 | 10 |
| 2023 | 0 | — | 0 | 8 |
| 2024 | 0 | — | 0 | 9 |
| 2025 | 0 | — | 0 | 7 |
| 2026 | 0 | — | 1 (1) | — |
https://510kreport.com/device/K904874 · printed Nov 5, 2026
Cite this page
510(k) Report. “K904874: Adjustable Peep Valve.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K904874
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026