K242346
- 510(k) number
- K242346
- Device name
- Grass® MR Conditional/CT Cup Electrodes
- Applicant
- Natus Manufacturing Limited IE
- Product code
- GXY — Electrode, Cutaneous
- Decision date
- 2024-08-29
- Date received
- 2024-08-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242346.pdf
Official FDA record: K242346
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.