K233364
- 510(k) number
- K233364
- Device name
- Axon Therapy
- Applicant
- Neuralace Medical, Inc. CA · US
- Product code
- QPL — Electromagnetic Stimulator, Pain Relief
- Decision date
- 2024-01-10
- Date received
- 2023-10-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K233364.pdf
Official FDA record: K233364
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.