K240788
- 510(k) number
- K240788
- Device name
- Ultrasound Stimulator
- Applicant
- Jkh Health Co., Ltd. CN
- Product code
- IMI — Ultrasonic Diathermy For Use In Applying Therapeutic
- Decision date
- 2025-06-04
- Date received
- 2024-03-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K240788.pdf
Official FDA record: K240788
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.