About This 510(k) Submission
K200296 is an FDA 510(k) clearance for the Pegavision (Etafilcon A) Color Daily Disposable Soft (Hydrophilic) Contact Lenses, Pegavision (Etafilcon A) Color Soft (Hydrophilic) Contact Lenses, a Lenses, Soft Contact, Daily Wear (Class II — Special Controls, product code LPL), submitted by Pegavision Corporation (Taoyuan City, TW). The FDA issued a Cleared decision on October 15, 2020, 252 days after receiving the submission on February 6, 2020. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.5925.