Clearance Summary
REFA, PHYSIOLOGICAL AMPLIFIER received FDA 510(k) clearance under submission number K060374, sponsored by Tms International BV. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2006-05-30.
- Submission: K060374
- Applicant / Sponsor: Tms International BV
- Clearance pathway: Abbreviated
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1835
- Decision date: 2006-05-30
Classification & Regulation
This clearance is catalogued under FDA product code GWL and 21 CFR 882.1835, within the Neurology review panel as a Class II device.