K240884
- 510(k) number
- K240884
- Device name
- Glide (91000-GL-X)
- Applicant
- Infinite Biomedical Technologies, LLC MD · US
- Product code
- GXY — Electrode, Cutaneous
- Decision date
- 2024-04-15
- Date received
- 2024-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K240884.pdf
Official FDA record: K240884
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.