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FDA 510(k)

OxySoft (olifilcon C) silicone hydrogel soft contact lens

K-Number: K191397 · 2019-10-02

Decision Date2019-10-02
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OxySoft (olifilcon C) silicone hydrogel soft contact lens is a medical device manufactured by Visco Vision, Inc.. It received FDA 510(k) clearance on 2019-10-02 under approval number K191397. 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 OxySoft (olifilcon C) silicone hydrogel soft contact lens?

OxySoft (olifilcon C) silicone hydrogel soft contact lens is a medical device that received FDA 510(k) clearance on 2019-10-02. It is manufactured by Visco Vision, Inc.. The 510(k) number is K191397.

When was OxySoft (olifilcon C) silicone hydrogel soft contact lens approved by the FDA?

OxySoft (olifilcon C) silicone hydrogel soft contact lens received FDA 510(k) clearance on 2019-10-02, under approval number K191397.

What company makes OxySoft (olifilcon C) silicone hydrogel soft contact lens?

OxySoft (olifilcon C) silicone hydrogel soft contact lens is manufactured by Visco Vision, Inc..

What is the FDA product code for OxySoft (olifilcon C) silicone hydrogel soft contact lens?

The FDA product code for OxySoft (olifilcon C) silicone hydrogel soft contact lens is LPL.

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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.