K241065
- 510(k) number
- K241065
- Device name
- ChecQ (AC100)
- Applicant
- Dentis Co., Ltd. KR
- Product code
- EKX — Handpiece, Direct Drive, Ac-Powered
- Decision date
- 2025-03-21
- Date received
- 2024-04-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K241065.pdf
Official FDA record: K241065
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.