Clearance Summary
ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000 received FDA 510(k) clearance under submission number K863815, sponsored by Elcot, 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 1987-06-02.
- Submission: K863815
- Applicant / Sponsor: Elcot, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5940
- Decision date: 1987-06-02
Classification & Regulation
This clearance is catalogued under FDA product code QGH and 21 CFR 882.5940, within the Neurology review panel as a Class II device.