K243495
- 510(k) number
- K243495
- Device name
- Natus Ultrapro S100 (982A0594)
- Applicant
- Natus Neurology Incorporated WI · US
- Product code
- GWF — Stimulator, Electrical, Evoked Response
- Decision date
- 2024-12-12
- Date received
- 2024-11-12
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K243495.pdf
Official FDA record: K243495
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.