K242161
- 510(k) number
- K242161
- Device name
- Radlink GPS Pro Imaging
- Applicant
- Radlink, Inc. CA · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-03-18
- Date received
- 2024-07-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K242161.pdf
Official FDA record: K242161
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.