K242175
- 510(k) number
- K242175
- Device name
- XOD Diathermia Radiofrequency Device
- Applicant
- Xod, Inc. PA · US
- Product code
- PBX — Massager, Vacuum, Radio Frequency Induced Heat
- Decision date
- 2025-02-27
- Date received
- 2024-07-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K242175.pdf
Official FDA record: K242175
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.