Clearance Summary
THE FM-212A BIOFEEDBACK UNIT received FDA 510(k) clearance under submission number K861950, sponsored by Hosa Technology, 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 1987-04-22.
- Submission: K861950
- Applicant / Sponsor: Hosa Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5050
- Decision date: 1987-04-22
Classification & Regulation
This clearance is catalogued under FDA product code HCC and 21 CFR 882.5050, within the Neurology review panel as a Class II device.