K233533
- 510(k) number
- K233533
- Device name
- NerveTape
- Applicant
- Biocircuit Technologies, Inc. GA · US
- Product code
- JXI — Cuff, Nerve
- Decision date
- 2024-02-12
- Date received
- 2023-11-02
- 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: K233533.pdf
Official FDA record: K233533
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.