K250286
- 510(k) number
- K250286
- Device name
- Rapid2 Magnetic Stimulators (Magstim Rapid2, Magstim Super Rapid2, Magstim Super Rapid2 Plus1)
- Applicant
- The Magstim Company Limited GB
- Product code
- QPL — Electromagnetic Stimulator, Pain Relief
- Decision date
- 2025-07-03
- Date received
- 2025-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K250286.pdf
Official FDA record: K250286
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.