Clearance Summary
PE-210AK SWITCH BOX received FDA 510(k) clearance under submission number K110376, sponsored by Nihon Kohden Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2011-07-29.
- Submission: K110376
- Applicant / Sponsor: Nihon Kohden Corp.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1400
- Decision date: 2011-07-29
Classification & Regulation
This clearance is catalogued under FDA product code GWQ and 21 CFR 882.1400, within the Neurology review panel as a Class II device.