K242500
- 510(k) number
- K242500
- Device name
- LARALAB
- Applicant
- Laralab GmbH DE
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-04-16
- Date received
- 2024-08-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K242500.pdf
Official FDA record: K242500
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.