510(k) · Cleared
ClearedAeroChamber2go Anti-Static Valved Holding Chamber
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Trudell Medical International · NVP Holding Chambers, Direct Patient Interface
Cleared on Jan 15, 2025 as substantially equivalent to K181649 (Trudell Medical International, 2019) after a 132-day review. Its family tree reaches back 2 generations to 2012.
- Decided
- Jan 15, 2025
- Review
- 132 days
- Class
- Class II
- Product code
- NVP
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K112010 (2012). No later device cites it as a predicate yet.
- Root · 2 generations backK112010 Aerochamber Plus Flow-VU Anti-Static Valved Holding Chamber (VHC)Trudell Medical Intl. · 2012
- 1 generation backK181649 AeroChamber Plus* Flow-Vu* Anti-Static Valved Holding Chamber (VHC)Trudell Medical International · 2019 · Recalled
- This deviceK242667 AeroChamber2go Anti-Static Valved Holding ChamberTrudell Medical International · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K112010 | Aerochamber Plus Flow-VU Anti-Static Valved Holding Chamber (VHC) | Trudell Medical Intl. | 2012 | — |
| −1 | K181649 | AeroChamber Plus* Flow-Vu* Anti-Static Valved Holding Chamber (VHC) | Trudell Medical International | 2019 | 1 |
| 0 (this device) | K242667 | AeroChamber2go Anti-Static Valved Holding Chamber | Trudell Medical International | 2025 | — |
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 NVP? 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 NVP device
- #1 K210558 LiteAire Basic Dual-Valved, Collapsible MDI…score 3.4 · 2 generations · no Class I recall
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 |
|---|---|---|---|
| * | K181649 | AeroChamber Plus* Flow-Vu* Anti-Static Valved Holding Chamber (VHC)Summary page 5…edical Specialty: Anesthesiology Regulation Number: 868.5630 Product Code(s): NVP 3. Legally Marketed Predicate Devices - 21 CFR 807.92(a)(3) Predicate Number: K181649 Predicate Trade Name: AeroChamber Plus* Flow-Vu* Anti-Static Valved Holding Chamber Common Name: Nebulizer Classificatio… | 2019 |
What descends from it?
No later submission names this one as a predicate yet.
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 13 years and passes through 2 companies; a new generation was cleared every 6.5 years on median.
- 1 of the 2 ancestors has a recall of any class.
How does its category compare?
All NVP devicesNVP Holding Chambers, Direct Patient Interface: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · NVP
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NVP
235in 2011
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NVP
No recall names NVP since 2007.
Adverse event reports per year · NVP
3in 2024
MAUDE reports naming product code NVP, 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 | — | 0 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 4 | 235 | 0 | 0 |
| 2012 | 1 | — | 0 | 0 |
| 2013 | 2 | — | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 2 |
| 2018 | 0 | — | 0 | 3 |
| 2019 | 1 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 1 |
| 2022 | 1 | — | 0 | 2 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 3 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
This product is intended to be used by patients (5+ years) who are under the care or treatment of a physician or licensed healthcare professional. The device is intended to be used by these patients to administer aerosolized medication from most pressurized Metered Dose Inhalers. It is a single patient, multiple use device intended for home use.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K242667 · printed Nov 6, 2026
Cite this page
510(k) Report. “K242667: AeroChamber2go Anti-Static Valved Holding Chamber.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K242667
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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