K232717
- 510(k) number
- K232717
- Device name
- Apex Locator (AL-Pex), Apex Locator (AL-Pex+)
- Applicant
- Changzhou Haili Medical Co., Ltd. CN
- Product code
- LQY — Locator, Root Apex
- Decision date
- 2023-12-22
- Date received
- 2023-09-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232717.pdf
Official FDA record: K232717
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.