K250376
- 510(k) number
- K250376
- Device name
- ViVY
- Applicant
- Viatherm Therapeutics, LLC PA · US
- Product code
- IMJ — Diathermy, Shortwave, For Use In Applying Therapeuti
- Decision date
- 2025-11-05
- Date received
- 2025-02-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K250376.pdf
Official FDA record: K250376
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.