K232649
- 510(k) number
- K232649
- Device name
- Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses
- Applicant
- Pegavision Corporation TW
- Product code
- LPL — Lenses, Soft Contact, Daily Wear
- Decision date
- 2024-05-08
- Date received
- 2023-08-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232649.pdf
Official FDA record: K232649
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.