510(k) DEN170024— AQUABEAM System
UnknownProcept Biorobotics, Corporation
Clearance details
- Applicant
- Procept Biorobotics, Corporation
- Product code
- Code PZP
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Redwood City, CA, US
Adverse events under product code PZP
product code PZP- Death
- 28
- Injury
- 622
- Malfunction
- 627
- Total
- 1,277
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.