K233856
- 510(k) number
- K233856
- Device name
- Precision1; Precision1 for Astigmatism; TOTAL30; TOTAL30 for Astigmatism; TOTAL30 Multifocal
- Applicant
- Alcon Laboratories, Inc. TX · US
- Product code
- LPL — Lenses, Soft Contact, Daily Wear
- Decision date
- 2023-12-29
- Date received
- 2023-12-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K233856.pdf
Official FDA record: K233856
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.