Clearance Summary
AQUABOND ELECTRODE received FDA 510(k) clearance under submission number K964433, sponsored by Medibond , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1997-01-27.
- Submission: K964433
- Applicant / Sponsor: Medibond , Ltd.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 1997-01-27
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.