K243339
- 510(k) number
- K243339
- Device name
- WiTOF
- Applicant
- Idmed FR
- Product code
- KOI — Stimulator, Nerve, Peripheral, Electric
- Decision date
- 2025-06-23
- Date received
- 2024-10-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
510(k) Summary (official FDA PDF): K243339.pdf
Official FDA record: K243339
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.