Clearance Summary
NH-2002 received FDA 510(k) clearance under submission number K932050, sponsored by New Horizon Health Care. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1995-06-05.
- Submission: K932050
- Applicant / Sponsor: New Horizon Health Care
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5800
- Decision date: 1995-06-05
Classification & Regulation
This clearance is catalogued under FDA product code QJQ and 21 CFR 882.5800, within the Neurology review panel as a Class II device.