Clearance Summary
GALAXY SYSTEM; JUPITER received FDA 510(k) clearance under submission number K111055, sponsored by Personal Health Institute International. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2011-12-21.
- Submission: K111055
- Applicant / Sponsor: Personal Health Institute International
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1400
- Decision date: 2011-12-21
Classification & Regulation
This clearance is catalogued under FDA product code OLV and 21 CFR 882.1400, within the Neurology review panel as a Class II device.