K242709
- 510(k) number
- K242709
- Device name
- JLK-PWI
- Applicant
- JLK, Inc. KR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-11-04
- Date received
- 2024-09-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K242709.pdf
Official FDA record: K242709
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.