Clearance Summary
KIMSTIM AURICULAR ELECTRODE received FDA 510(k) clearance under submission number K011691, sponsored by Kim Institute For Rehabilitation Medicine, P.C.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2001-12-27.
- Submission: K011691
- Applicant / Sponsor: Kim Institute For Rehabilitation Medicine, P.C.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 2001-12-27
Classification & Regulation
This clearance is catalogued under FDA product code GXY and 21 CFR 882.1320, within the Neurology review panel as a Class II device.