510(k) · Cleared
ClearedNeuronaute
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Bioserenity Sas · GWQ Full-Montage Standard Electroencephalograph
Cleared on Dec 10, 2020 as substantially equivalent to K183529 (Nihon Kohden Corporation, 2019) after a 115-day review. Its family tree reaches back 3 generations to 1983. 4 later devices descend from it.
- Decided
- Dec 10, 2020
- Review
- 115 days
- Class
- Class II
- Product code
- GWQ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K830295 (1983). 5 ancestors in all. 4 later devices descend from it, 2 citing it directly.
- Root · 3 generations backK830295 Medilog 9000 SystemOxford Medilog, Inc. · 1983
- 2 generations backK170363 Ceribell Pocket EEG DeviceCeribell, Inc. · 2017
- 1 generation backK183529 AE-120A EEG Head SetNihon Kohden Corporation · 2019
- This deviceK202334 NeuronauteBioserenity Sas · 2020
- Descendant · cites it directly · 1 of its ownK231366 Neuronaute PlusBioserenity Sas · 2023
- Descendant · cites it directly · 1 of its ownK223644 Neuronaute with IceCap 2 & IceCap 2 SmallBioserenity · 2023
- Descendant · 2 generations on · 0 of its ownK261101 Ceribell MonitorCeribell, Inc. · 2026
- Descendant · 2 generations on · 0 of its ownK243788 IceCap product lineBioserenity Medical Devices Group · 2025
Most influential descendants
Showing 4 of 4 · See all- K231366Neuronaute PlusBioserenity Sas · 2023 · cites it directly1descendant
- K223644Neuronaute with IceCap 2 & IceCap 2 SmallBioserenity · 2023 · cites it directly1descendant
- K261101Ceribell MonitorCeribell, Inc. · 2026 · 2 generations on0descendants
- K243788IceCap product lineBioserenity Medical Devices Group · 2025 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K830295 | Medilog 9000 System | Oxford Medilog, Inc. | 1983 | — |
| −2 | K170363 | Ceribell Pocket EEG Device | Ceribell, Inc. | 2017 | — |
| −1 | K183529 | AE-120A EEG Head Set | Nihon Kohden Corporation | 2019 | — |
| 0 (this device) | K202334 | Neuronaute | Bioserenity Sas | 2020 | — |
| +1 | K231366 | Neuronaute Plus | Bioserenity Sas | 2023 | — |
| +1 | K223644 | Neuronaute with IceCap 2 & IceCap 2 Small | Bioserenity | 2023 | — |
| +2 | K261101 | Ceribell Monitor | Ceribell, Inc. | 2026 | — |
| +2 | K243788 | IceCap product line | Bioserenity Medical Devices Group | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 1 | 0 |
| 2017 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2023 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 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.
Planning a device in GWQ? 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 GWQ device
- #1 K260455 New Wave Systemscore 13.7 · 10 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 |
|---|---|---|---|
| * | K183529 | AE-120A EEG Head SetSummary page 5…am Device Class: II Page 1 of 20 Predicate Device Information K183529 Device Name AE-120A EEG Head Set Manufacturer Nihon Kohden Corporation… | 2019 |
| † | K072016 | Cup Electrodes, Gold, Reusable, Silver, Reusable; Cup Electrodes Silver/Silver Chloride… | 2007 |
| † | K860210 | Elefix Electrode Cream | 1986 |
| † | K170441 | ElectroTek | 2017 |
| † | K010460 | Lifelines Trackit | 2001 |
What descends from it? (4)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 37 years and passes through 4 companies; a new generation was cleared every 1.9 years on median.
- None of the 5 ancestors has a recall.
- Of its descendants, K231366 (Bioserenity Sas, 2023) has gone furthest, with 1 descendant of its own.
- 2 other devices also cite its predicate K183529.
How does its category compare?
All GWQ devicesGWQ Full-Montage Standard Electroencephalograph: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · GWQ
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · GWQ
137in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GWQ
1in 2020
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GWQ
13in 2025
MAUDE reports naming product code GWQ, 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 | — | 5 | 11 |
| 2008 | 2 | — | 2 | 8 |
| 2009 | 0 | — | 1 | 7 |
| 2010 | 3 | 73 | 1 | 12 |
| 2011 | 4 | 220 | 0 | 6 |
| 2012 | 4 | 208 | 0 | 9 |
| 2013 | 2 | — | 0 | 4 |
| 2014 | 2 | — | 0 | 7 |
| 2015 | 3 | 276 | 2 | 13 |
| 2016 | 3 | 50 | 0 | 28 |
| 2017 | 5 | 181 | 0 | 17 |
| 2018 | 8 | 150 | 0 | 15 |
| 2019 | 0 | — | 2 | 16 |
| 2020 | 6 | 216 | 1 | 30 |
| 2021 | 0 | — | 0 | 20 |
| 2022 | 3 | 216 | 0 | 16 |
| 2023 | 6 | 137 | 0 | 20 |
| 2024 | 1 | — | 0 | 17 |
| 2025 | 0 | — | 0 | 13 |
| 2026 | 2 | — | 1 | — |
What is it indicated for?
Neuronaute is a system intended to acquire, display, store, archive, and periodically transmit EEG signals from the brain using a full montage array to enable review at a physician’s office, hospital, or other remote locations. It allows remote access by users via the Neuronaute N-CLOUD which receives EEG signals from Neuronaute Head Module which sends transmissions to the cloud. Neuronaute and its associated software are intended to assist in the…
Read the full statement (159 words)
Neuronaute is a system intended to acquire, display, store, archive, and periodically transmit EEG signals from the brain using a full montage array to enable review at a physician’s office, hospital, or other remote locations. It allows remote access by users via the Neuronaute N-CLOUD which receives EEG signals from Neuronaute Head Module which sends transmissions to the cloud. Neuronaute and its associated software are intended to assist in the diagnosis of neurological disorders. Neuronaute and its components do not provide any diagnostics conclusions or automated alerts of an adverse clinical event about a patient's clinical condition.
The device is for use by trained medical professionals for patients under medical supervision. The device is intended for use on adults (ages 18 and above). Neuronaute is not intended to replace direct communication with healthcare providers. The system data should not be used alone, but should be used along with all other clinical data and exams to come to a diagnosis.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K202334 · printed Nov 6, 2026
Cite this page
510(k) Report. “K202334: Neuronaute.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202334
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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