K240385
- 510(k) number
- K240385
- Device name
- VINT
- Applicant
- Mediimg Corporation KR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-10-15
- Date received
- 2024-02-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K240385.pdf
Official FDA record: K240385
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.