Clearance Summary
LSI SYSTEM II received FDA 510(k) clearance under submission number K904743, sponsored by M.S.P. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1991-09-04.
- Submission: K904743
- Applicant / Sponsor: M.S.P. , Ltd.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5890
- Decision date: 1991-09-04
Classification & Regulation
This clearance is catalogued under FDA product code LIH and 21 CFR 882.5890, within the Neurology review panel as a Class II device.