K241952
- 510(k) number
- K241952
- Device name
- AQUABEAM Robotic System (AB2000)
- Applicant
- Procept Biorobotics CA · US
- Product code
- PZP — Fluid Jet Removal System
- Decision date
- 2024-09-30
- Date received
- 2024-07-03
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K241952.pdf
Official FDA record: K241952
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.