510(k) Report

De Novo · Granted

Granted

Neba System

DEN110019De NovoGranted Jul 15, 2013585-day reviewClass II21 CFR 882.1440

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Lexicor Medical Technology, LLC · NCG Neuropsychiatric Interpretative Electroencephalograph Assessment Aid

Granted on Jul 15, 2013 as a new device type through De Novo after a 585-day review. 2 later devices descend from it.

Decided
Jul 15, 2013
Review
585 days
Class
Class II
Product code
NCG
Recalls
None

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2023: 1 descendant cleared2025: 1 descendant cleared2010201520202025
  1. This deviceDEN110019 Neba SystemLexicor Medical Technology, LLC · 2013
  2. Descendant · cites it directly · 1 of its ownK222680 DeltaScan MonitorProlira B.V. · 2023
  3. Descendant · 2 generations on · 0 of its ownK251936 Ceribell Delirium Monitor SystemCeribell, Inc. · 2025

Most influential descendants

Showing 2 of 2 · See all
  • K222680DeltaScan MonitorProlira B.V. · 2023 · cites it directly1descendant
  • K251936Ceribell Delirium Monitor SystemCeribell, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)DEN110019Neba SystemLexicor Medical Technology, LLC2013—
+1K222680DeltaScan MonitorProlira B.V.2023—
+2K251936Ceribell Delirium Monitor SystemCeribell, Inc.2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202510
FIG. 1 — Lineage of DEN110019, 2013–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA De Novo 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 NCG? 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 NCG device

  1. #1 K251936 Ceribell Delirium Monitor Systemscore 12.3 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

Does it have a predicate?

De Novo decisions do not claim a predicate device.

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K222680DeltaScan MonitorProlira B.V.20231

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, K222680 (Prolira B.V., 2023) has gone furthest, with 1 descendant of its own.

How does its category compare?

All NCG devices

NCG Neuropsychiatric Interpretative Electroencephalograph Assessment Aid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · NCG

1in 2025

2013: 12023: 12025: 1
2007high 1 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NCG

Too few NCG 510(k)s in any year since 2007 to give a median.

Recalls per year · NCG

No recall names NCG since 2007.

Adverse event reports per year · NCG

No MAUDE report names NCG since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20131—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20231—00
20240—00
20251—00
20260—0—
Cite this page

510(k) Report. “DEN110019: Neba System.” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN110019

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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