K232152
- 510(k) number
- K232152
- Device name
- NerivioInfinity
- Applicant
- Theranica Bioelectronics , Ltd. IL
- Product code
- QGT — Distal Transcutaneous Electrical Stimulator For Trea
- Decision date
- 2023-11-08
- Date received
- 2023-07-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232152.pdf
Official FDA record: K232152
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.