K233599
- 510(k) number
- K233599
- Device name
- X-Clever (ASHK100G)
- Applicant
- Lg Electronics.Inc KR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-03-18
- Date received
- 2023-11-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233599.pdf
Official FDA record: K233599
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.