K241789
- 510(k) number
- K241789
- Device name
- Non-Sterile Ultrasound Transmission Gels
- Applicant
- Hony Medical Co., Ltd. CN
- Product code
- MUI — Media, Coupling, Ultrasound
- Decision date
- 2024-07-24
- Date received
- 2024-06-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241789.pdf
Official FDA record: K241789
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.