K242305
- 510(k) number
- K242305
- Device name
- BE Plus PRO, Neurotravel LIGHT
- Applicant
- Eb Neuro S.P.A. IT
- Product code
- GWL — Amplifier, Physiological Signal
- Decision date
- 2024-09-04
- Date received
- 2024-08-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.4 MB · U.S. public domain
Also available from FDA: K242305.pdf
Official FDA record: K242305
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.