K233902
- 510(k) number
- K233902
- Device name
- Centurion Vision System (Active Sentry) (8065753057)
- Applicant
- Alcon Laboratories, Inc. TX · US
- Product code
- HQC — Unit, Phacofragmentation
- Decision date
- 2024-01-10
- Date received
- 2023-12-11
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K233902.pdf
Official FDA record: K233902
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.