K233885
- 510(k) number
- K233885
- Device name
- rainbow Paste Stain SE
- Applicant
- Genoss Co., Ltd. KR
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2024-06-21
- Date received
- 2023-12-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233885.pdf
Official FDA record: K233885
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.