Clearance Summary
RAINBOW GT-4A PAIN RELIEF MACHINE received FDA 510(k) clearance under submission number K031546, sponsored by Sino-Us Information, 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 2003-11-13.
- Submission: K031546
- Applicant / Sponsor: Sino-Us Information, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5890
- Decision date: 2003-11-13
Classification & Regulation
This clearance is catalogued under FDA product code GZJ and 21 CFR 882.5890, within the Neurology review panel as a Class II device.