K233582
- 510(k) number
- K233582
- Device name
- Rapid
- Applicant
- Ischemaview, Inc. CO · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-04-22
- Date received
- 2023-11-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233582.pdf
Official FDA record: K233582
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.