K233512
- 510(k) number
- K233512
- Device name
- Rapid (6.0)
- Applicant
- Ischemaview, Inc. CO · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-01-16
- Date received
- 2023-11-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K233512.pdf
Official FDA record: K233512
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.