AQUASPLASH(聚甲基丙烯酸甲酯)软性(亲水性)日戴隐形眼镜
K号: K210609 · 2021-04-27
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器械摘要
常见问题
What is the AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens?
AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens is a medical device that received FDA 510(k) clearance on 2021-04-27. The listed applicant is Vp Optics. The 510(k) number is K210609.
When did AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens receive FDA 510(k) clearance?
AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens received FDA 510(k) clearance on 2021-04-27, under 510(k) number K210609.
Who is the listed applicant for AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens?
The FDA 510(k) record lists Vp Optics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens?
The FDA product code for AQUASPLASH (Polymacon) 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。
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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