K232174
- 510(k) number
- K232174
- Device name
- rainbowTM Multi-Layer Block / bright 3-Layer / bright Mono
- Applicant
- Genoss Co., Ltd. KR
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2024-02-23
- Date received
- 2023-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232174.pdf
Official FDA record: K232174
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.