K240632
- 510(k) number
- K240632
- Device name
- Neuvotion NeuStim NN-01
- Applicant
- Neuvotion, Inc. CT · US
- Product code
- GZI — Stimulator, Neuromuscular, External Functional
- Decision date
- 2024-11-22
- Date received
- 2024-03-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K240632.pdf
Official FDA record: K240632
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.