K233322
- 510(k) number
- K233322
- Device name
- Mochida Nerve Cuff
- Applicant
- Mochida Pharmaceutical Co., Ltd. JP
- Product code
- JXI — Cuff, Nerve
- Decision date
- 2024-06-21
- Date received
- 2023-09-29
- 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: K233322.pdf
Official FDA record: K233322
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.