Lucens 41(senofilcon C)硅水凝胶软(亲水性)隐形眼镜
K号: K242391 · 2024-10-08
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器械摘要
常见问题
What is the Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens?
Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens is a medical device that received FDA 510(k) clearance on 2024-10-08. The listed applicant is Lucens Technology Co., Ltd.. The 510(k) number is K242391.
When did Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens receive FDA 510(k) clearance?
Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens received FDA 510(k) clearance on 2024-10-08, under 510(k) number K242391.
Who is the listed applicant for Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens?
The FDA 510(k) record lists Lucens Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens?
The FDA product code for Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) 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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