Oasis 泪点插管套装
K号: K160710 · 2016-05-13
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器械摘要
Oasis Lacrimal Intubation Set is the device name listed in this FDA 510(k) record. The listed applicant is Anodyne. It received FDA 510(k) clearance on 2016-05-13 under 510(k) number K160710. The device is classified under product code OKS. FDA Decision: Unknown.
常见问题
What is the Oasis Lacrimal Intubation Set?
Oasis Lacrimal Intubation Set is a medical device that received FDA 510(k) clearance on 2016-05-13. The listed applicant is Anodyne. The 510(k) number is K160710.
When did Oasis Lacrimal Intubation Set receive FDA 510(k) clearance?
Oasis Lacrimal Intubation Set received FDA 510(k) clearance on 2016-05-13, under 510(k) number K160710.
Who is the listed applicant for Oasis Lacrimal Intubation Set?
The FDA 510(k) record lists Anodyne as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Oasis Lacrimal Intubation Set?
The FDA product code for Oasis Lacrimal Intubation Set is OKS.
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：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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