K232210
- 510(k) number
- K232210
- Device name
- X-trodes System M
- Applicant
- X-Trodes IL
- Product code
- GWL — Amplifier, Physiological Signal
- Decision date
- 2024-02-04
- Date received
- 2023-07-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232210.pdf
Official FDA record: K232210
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.