510(k) · Cleared

Cleared

Brainet Kit

K043009510(k) TraditionalCleared Jan 12, 200572-day reviewClass II21 CFR 882.1320

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

Jordan Neuroscience, Inc. · GXY Electrode, Cutaneous

Cleared on Jan 12, 2005 as substantially equivalent to K780045 (Electro-Cap Intl., Inc., 1978) after a 72-day review. Its family tree reaches back 1 generation to 1978. 1 later device descends from it.

Decided: Jan 12, 2005
Review: 72 days
Class: Class II
Product code: GXY
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K780045 (1978). 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 1 generation backK780045 Electrode CapElectro-Cap Intl., Inc. · 1978
This deviceK043009 Brainet KitJordan Neuroscience, Inc. · 2005
Descendant · cites it directly · 0 of its ownK191225 EEG Electrode TemplateRhythmlink International, LLC · 2019

Most influential descendants

Showing 1 of 1 · See all

K191225EEG Electrode TemplateRhythmlink International, LLC · 2019 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K780045	Electrode Cap	Electro-Cap Intl., Inc.	1978	—
0 (this device)	K043009	Brainet Kit	Jordan Neuroscience, Inc.	2005	—
+1	K191225	EEG Electrode Template	Rhythmlink International, LLC	2019	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2019	1	0

FIG. 1 — Lineage of K043009, 1978–2019Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 GXY? 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 GXY device

#1 K232052 Ceribell Instant EEG Headbandscore 16.3 · 6 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (2)

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	Applicant	Decided	Recalls
*	K780045	Electrode Cap Summary page 1 …electrodes Classification Name: 21 CFR 882.1320; Product Code: GXY Predicate Device: 5 10(k) Number: K780045 Manufacture: Electro-Cap International Trade Name…	Electro-Cap Intl., Inc.	1978	—
*	—	AMBU Disposable Cup Electrode Named without a submission number			—

Also cleared against K780045: 7 other devices →

What descends from it? (1)

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

Number	Device	Applicant	Decided	Descendants
K191225	EEG Electrode Template	Rhythmlink International, LLC	2019	0

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?

Its one ancestor has no recall.
Of its descendants, K191225 (Rhythmlink International, LLC, 2019) has gone furthest, with 0 descendants of its own.
7 other devices also cite its predicate K780045.

How does its category compare?

All GXY devices

GXY Electrode, Cutaneous: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GXY

6in 2025

2007high 17 (2009) · low 3 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GXY

148in 2025

2007high 203 (2014) · low 81 (2022)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GXY

2in 2023

2007high 5 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · GXY

58in 2025

2007high 58 (2025) · low 10 (2018)2025

MAUDE reports naming product code GXY, 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	7	88	0	14
2008	9	136	0	17
2009	17	159	4	15
2010	3	137	1	14
2011	6	183	5	16
2012	9	150	4	16
2013	7	99	0	15
2014	9	203	0	11
2015	6	119	0	19
2016	6	170	0	15
2017	9	116	0	11
2018	14	135	0	10
2019	9	113	0	19
2020	4	108	0	11
2021	12	195	0	21
2022	5	81	0	34
2023	13	132	2	25
2024	7	111	0	51
2025	6	148	0	58
2026	12	70	0	—

What is it indicated for?

The BraiNet® Kit contents are placed on the scalp to support electroencephalograph (EEG) electrode placement.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K043009 · printed Nov 6, 2026

Cite this page

510(k) Report. “K043009: Brainet Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K043009

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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