K242386
- 510(k) number
- K242386
- Device name
- Bluemoon
- Applicant
- Genoss Co., Ltd. CN
- Product code
- EBZ — Activator, Ultraviolet, For Polymerization
- Decision date
- 2025-05-05
- Date received
- 2024-08-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 4.1 MB · U.S. public domain
Also available from FDA: K242386.pdf
Official FDA record: K242386
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.