FDA 510(k)

ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color)

K-Number: K161098 · 2016-08-22

Decision Date2016-08-22

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color) is the device name listed in this FDA 510(k) record. The listed applicant is Joowon Innovation Co., Ltd.. It received FDA 510(k) clearance on 2016-08-22 under 510(k) number K161098. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color)?

ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color) is a medical device that received FDA 510(k) clearance on 2016-08-22. The listed applicant is Joowon Innovation Co., Ltd.. The 510(k) number is K161098.

When did ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color) receive FDA 510(k) clearance?

ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color) received FDA 510(k) clearance on 2016-08-22, under 510(k) number K161098.

Who is the listed applicant for ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color)?

The FDA 510(k) record lists Joowon Innovation Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color)?

The FDA product code for ChicView (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Tinted/Color) 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.

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Related Devices (Code: LPL)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.