Clearance Summary
POST-OP ELECTRODE (TENS ELECTRODE) received FDA 510(k) clearance under submission number K820082, sponsored by Consolidated Medical Equipment, 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 1982-01-28.
- Submission: K820082
- Applicant / Sponsor: Consolidated Medical Equipment, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 1982-01-28
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.