K240707
- 510(k) number
- K240707
- Device name
- Ultrasonic Scaler (WD-JY-B002,WD-JY-W001,WD-JY-R003,WD-JY-G004,WD-JY-B003,WD-JY-C006,WD-JY-M0014, WD-JY-N0015,WD-JY-N0016,WD-JY-N0017,WD-JY-E007, WD-JY-F008,WD-JY-A005,WD-JY-H009,WD-JY-I0011, WD-JY-K0012,WD-JY-K0013,WD-JY-K0014, WD-JY-L0013,WD-JY-L0014,WD-JY-L0015, WD-JY-L0016,WD-JY-L0017)
- Applicant
- Shenzhen Micro Electric Intelligence Co., Ltd. CN
- Product code
- ELC — Scaler, Ultrasonic
- Decision date
- 2024-07-02
- Date received
- 2024-03-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K240707.pdf
Official FDA record: K240707
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.