K241719
- 510(k) number
- K241719
- Device name
- NeuroICH
- Applicant
- Neurocareai, Inc. TX · US
- Product code
- QAS — Radiological Computer-Assisted Triage And Notificati
- Decision date
- 2024-11-07
- Date received
- 2024-06-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K241719.pdf
Official FDA record: K241719
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.