K233921
- 510(k) number
- K233921
- Device name
- Luvis Chair (LC700C)
- Applicant
- Dentis Co., Ltd. KR
- Product code
- KLC — Chair, Dental, With Operative Unit
- Decision date
- 2024-09-06
- Date received
- 2023-12-13
- 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: K233921.pdf
Official FDA record: K233921
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.