Clearance Summary
TENS CONDUCTIVE MEDIA PAD received FDA 510(k) clearance under submission number K853633, sponsored by Alternative Design Systems, 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 1985-12-03.
- Submission: K853633
- Applicant / Sponsor: Alternative Design Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 1985-12-03
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.