K230895
- 510(k) number
- K230895
- Device name
- CEFLA Dental Micromotors: i-MMr, i-MMr L, i-MMr L FLUO, i-MMs, i-MMs FLUO; i-XR3, i-XR3 L, i-XR3 L FLUO, i-XS4,
- Applicant
- Cefla S.C. IT
- Product code
- EBW — Controller, Foot, Handpiece And Cord
- Decision date
- 2024-04-01
- Date received
- 2023-03-31
- 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: K230895.pdf
Official FDA record: K230895
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.