K243789
- 510(k) number
- K243789
- Device name
- LIBERTY Endovascular Robotic System (LIBERTYOS)
- Applicant
- Microbot Medical , Ltd. IL
- Product code
- DXX — System, Catheter Control, Steerable
- Decision date
- 2025-09-04
- Date received
- 2024-12-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K243789.pdf
Official FDA record: K243789
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.