Clearance Summary
RHS HELMET received FDA 510(k) clearance under submission number K012007, sponsored by Restorative Health Svs, 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 2001-09-19.
- Submission: K012007
- Applicant / Sponsor: Restorative Health Svs, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5970
- Decision date: 2001-09-19
Classification & Regulation
This clearance is catalogued under FDA product code MVA and 21 CFR 882.5970, within the Neurology review panel as a Class II device.