K233211
- 510(k) number
- K233211
- Device name
- AVIEW CAC
- Applicant
- Coreline Soft Co., Ltd. KR
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-03-29
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233211.pdf
Official FDA record: K233211
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.