Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses
K-Number: K232649 · 2024-05-08
Device Summary
Frequently Asked Questions
What is the Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses?
Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses is a medical device that received FDA 510(k) clearance on 2024-05-08. It is manufactured by Pegavision Corporation. The 510(k) number is K232649.
When was Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses approved by the FDA?
Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses received FDA 510(k) clearance on 2024-05-08, under approval number K232649.
What company makes Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses?
Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses is manufactured by Pegavision Corporation.
What is the FDA product code for Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses?
The FDA product code for Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses is LPL.
Related Clinical Trials
Other Devices by Pegavision Corporation
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.