K231575
- 510(k) number
- K231575
- Device name
- Vecttor VT-300
- Applicant
- Artaflex, Inc. CA
- Product code
- LIH — Interferential Current Therapy
- Decision date
- 2024-02-08
- Date received
- 2023-05-31
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231575.pdf
Official FDA record: K231575
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.