K253211
- 510(k) number
- K253211
- Device name
- AQUABEAM Robotic System
- Applicant
- Procept Biorobotics CA · US
- Product code
- PZP — Fluid Jet Removal System
- Decision date
- 2026-06-23
- Date received
- 2025-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253211.pdf
Official FDA record: K253211
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.