NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses
K-Number: K173086 · 2017-11-07
Device Summary
Frequently Asked Questions
What is the NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses?
NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses is a medical device that received FDA 510(k) clearance on 2017-11-07. The listed applicant is Visioneering Technologies, Inc.. The 510(k) number is K173086.
When did NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses receive FDA 510(k) clearance?
NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses received FDA 510(k) clearance on 2017-11-07, under 510(k) number K173086.
Who is the listed applicant for NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses?
The FDA 510(k) record lists Visioneering Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses?
The FDA product code for NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses is LPL.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LPL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.