Clearance Summary
RAINBOW BLOCK received FDA 510(k) clearance under submission number K092513, sponsored by Genoss Co., Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-10-09.
- Submission: K092513
- Applicant / Sponsor: Genoss Co., Ltd.
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2009-10-09
Classification & Regulation
This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.