Lacriflow CL
K号: K170247 · 2017-04-18
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器械摘要
Lacriflow CL is the device name listed in this FDA 510(k) record. The listed applicant is Kaneka Pharma America, LLC. It received FDA 510(k) clearance on 2017-04-18 under 510(k) number K170247. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.
常见问题
What is the Lacriflow CL?
Lacriflow CL is a medical device that received FDA 510(k) clearance on 2017-04-18. The listed applicant is Kaneka Pharma America, LLC. The 510(k) number is K170247.
When did Lacriflow CL receive FDA 510(k) clearance?
Lacriflow CL received FDA 510(k) clearance on 2017-04-18, under 510(k) number K170247.
Who is the listed applicant for Lacriflow CL?
The FDA 510(k) record lists Kaneka Pharma America, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lacriflow CL?
The FDA product code for Lacriflow CL is OKS.
相关临床试验
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列明Kaneka Pharma America, LLC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：OKS）
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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