K241045
- 510(k) number
- K241045
- Device name
- Disposable Subdermal Needle Electrode, Corkscrew
- Applicant
- Technomed Europe NL
- Product code
- GXZ — Electrode, Needle
- Decision date
- 2024-12-11
- Date received
- 2024-04-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K241045.pdf
Official FDA record: K241045
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.