Clearance Summary
NEUROSIGN LARYNGEAL ELECTRODES received FDA 510(k) clearance under submission number K071349, sponsored by The Magstim Company , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2007-12-12.
- Submission: K071349
- Applicant / Sponsor: The Magstim Company , Ltd.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1820
- Decision date: 2007-12-12
Classification & Regulation
This clearance is catalogued under FDA product code ETN and 21 CFR 874.1820, within the Ear, Nose, Throat review panel as a Class II device.