# K242305: BE Plus PRO, Neurotravel LIGHT

- Pathway: 510(k) (Special)
- Applicant: Eb Neuro S.P.A.
- Decided: Sep 4, 2024 after 30 days
- Product code: GWL (Amplifier, Physiological Signal)
- Device class: 2
- Regulation: 21 CFR 882.1835
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K003154 (2001). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121996: BE Plus LTM Amplifier Gwi Amplifier, Eb Neuro S.P.A. (2012) Summary page 5.
- K142064: Galileo NT, Eb Neuro S.P.A. (2015) Summary page 5.

## Indications for use
BE Plus PRO and Neurotravel LIGHT are intended to be used for Electroencephalography (EEG) and Polysomnography (PSG) exams, in combination with the Galileo NT Line software, for human beings to assist the user in diagnosis and monitoring of disorders of the central and peripheral nervous system and muscles.

Source page: https://510kreport.com/device/K242305
Methodology: https://510kreport.com/methodology