Clearance Summary
DUAL TYPE ELECTRODE received FDA 510(k) clearance under submission number K810206, sponsored by Professional Instruments Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1981-03-20.
- Submission: K810206
- Applicant / Sponsor: Professional Instruments Co.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 1981-03-20
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.