K240519
- 510(k) number
- K240519
- Device name
- Innova Vision (inifilcon A) Silicone Hydrogel (Hydrophilic) Daily Wear Soft Contact Lens
- Applicant
- Innova Vision, Inc. TW
- Product code
- LPL — Lenses, Soft Contact, Daily Wear
- Decision date
- 2024-04-17
- Date received
- 2024-02-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
510(k) Summary (official FDA PDF): K240519.pdf
Official FDA record: K240519
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.