Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens
K号: K213216 · 2022-01-18
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器械摘要
常见问题
What is the Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?
Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is a medical device that received FDA 510(k) clearance on 2022-01-18. The listed applicant is Unicon Optical Co., Ltd.. The 510(k) number is K213216.
When did Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens receive FDA 510(k) clearance?
Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens received FDA 510(k) clearance on 2022-01-18, under 510(k) number K213216.
Who is the listed applicant for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?
The FDA 510(k) record lists Unicon Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?
The FDA product code for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is LPL.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
列明Unicon Optical Co., Ltd.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:LPL)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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