Clearance Summary
SUBDERMAL WIRE ELECTRODE, MODEL SWE received FDA 510(k) clearance under submission number K062880, sponsored by Ives Eeg Solutions, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2006-12-22.
- Submission: K062880
- Applicant / Sponsor: Ives Eeg Solutions, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1350
- Decision date: 2006-12-22
Classification & Regulation
This clearance is catalogued under FDA product code GXZ and 21 CFR 882.1350, within the Neurology review panel as a Class II device.