K241267
- 510(k) number
- K241267
- Device name
- Hidroxa SE30
- Applicant
- Hidroxa Medical AB SE
- Product code
- EGJ — Device, Iontophoresis, Other Uses
- Decision date
- 2024-10-17
- Date received
- 2024-05-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K241267.pdf
Official FDA record: K241267
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.