510(k) · Cleared
ClearedCurry Multimodal Neuroimaging Software
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Neurosoft, Inc. · OLX Source Localization Software For Electroencephalograph Or Magnetoencephalograph
Cleared on Feb 5, 2001 after a 237-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 6 later devices descend from it.
- Decided
- Feb 5, 2001
- Review
- 237 days
- Class
- Class II
- Product code
- OLX
- Recalls
- None
- Predicates
- 0
6 later devices descend from it, 3 citing it directly.
- This deviceK001781 Curry Multimodal Neuroimaging SoftwareNeurosoft, Inc. · 2001
- Descendant · cites it directly · 4 of its ownK092844 GeosourceElectrical Geodesics, Inc. · 2010
- Descendant · cites it directly · 2 of its ownK172858 PreOpEpilog · 2018
- Descendant · 2 generations on · 0 of its ownK252565 PreOp v3Clouds of Care · 2026
- Descendant · 2 generations on · 0 of its ownK250239 NeuroMatchLVIS Corporation · 2025
- Descendant · 2 generations on · 0 of its ownK241513 SourcererBrain Electrophysiology Laboratory Company, LLC · 2024
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K092844GeosourceElectrical Geodesics, Inc. · 2010 · cites it directly4descendants
- K172858PreOpEpilog · 2018 · cites it directly2descendants
- K252565PreOp v3Clouds of Care · 2026 · 2 generations on0descendants
- K250239NeuroMatchLVIS Corporation · 2025 · 2 generations on0descendants
- K241513SourcererBrain Electrophysiology Laboratory Company, LLC · 2024 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K001781 | Curry Multimodal Neuroimaging Software | Neurosoft, Inc. | 2001 | — |
| +1 | K092844 | Geosource | Electrical Geodesics, Inc. | 2010 | — |
| +1 | K172858 | PreOp | Epilog | 2018 | — |
| +2 | K252565 | PreOp v3 | Clouds of Care | 2026 | — |
| +2 | K250239 | NeuroMatch | LVIS Corporation | 2025 | — |
| +2 | K241513 | Sourcerer | Brain Electrophysiology Laboratory Company, LLC | 2024 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 1 | 0 |
| 2015 | 1 | 0 |
| 2018 | 1 | 0 |
| 2024 | 1 | 0 |
| 2025 | 1 | 0 |
| 2026 | 1 | 0 |
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.
Planning a device in OLX? 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 OLX device
- #1 K260563 CN-Suite™score 13.9 · 8 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin 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? (6)
3 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?
- Of its descendants, K092844 (Electrical Geodesics, Inc., 2010) has gone furthest, with 4 descendants of its own.
How does its category compare?
All OLX devicesOLX Source Localization Software For Electroencephalograph Or Magnetoencephalograph: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · OLX
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OLX
462in 2010
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OLX
No recall names OLX since 2007.
Adverse event reports per year · OLX
1in 2015
MAUDE reports naming product code OLX, 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 | 3 | 462 | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 1 |
| 2015 | 0 | — | 0 | 1 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 2 | — | 0 | 0 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 2 | — | 0 | — |
https://510kreport.com/device/K001781 · printed Nov 6, 2026
Cite this page
510(k) Report. “K001781: Curry Multimodal Neuroimaging Software.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K001781
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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