K251533
- 510(k) number
- K251533
- Device name
- Rapid Obstructive Hydrocephalus, Rapid OH
- Applicant
- Ischemaview, Inc. CO · US
- Product code
- QAS — Radiological Computer-Assisted Triage And Notificati
- Decision date
- 2025-09-04
- Date received
- 2025-05-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251533.pdf
Official FDA record: K251533
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.