K231990
- 510(k) number
- K231990
- Device name
- Apex Locator
- Applicant
- Cefla S.C. IT
- Product code
- LQY — Locator, Root Apex
- Decision date
- 2024-02-13
- Date received
- 2023-07-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K231990.pdf
Official FDA record: K231990
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.