K233221
- 510(k) number
- K233221
- Device name
- Metro Soft, Silicone Hydrogel Daily Wear Soft Contact Lens (efrofilcon A)
- Applicant
- Metro Optics of Austin, Inc. TX · US
- Product code
- LPL — Lenses, Soft Contact, Daily Wear
- Decision date
- 2024-02-06
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K233221.pdf
Official FDA record: K233221
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.