Decision Date2016-10-24
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Visco (olifilcon A) soft contact lens is a medical device manufactured by Visco Vision, Inc.. It received FDA 510(k) clearance on 2016-10-24 under approval number K160245. 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 Visco (olifilcon A) soft contact lens?
Visco (olifilcon A) soft contact lens is a medical device that received FDA 510(k) clearance on 2016-10-24. It is manufactured by Visco Vision, Inc.. The 510(k) number is K160245.
When was Visco (olifilcon A) soft contact lens approved by the FDA?
Visco (olifilcon A) soft contact lens received FDA 510(k) clearance on 2016-10-24, under approval number K160245.
What company makes Visco (olifilcon A) soft contact lens?
Visco (olifilcon A) soft contact lens is manufactured by Visco Vision, Inc..
What is the FDA product code for Visco (olifilcon A) soft contact lens?
The FDA product code for Visco (olifilcon A) soft contact lens is LPL.
Related Devices (Code: 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.