UniTex 非无菌、无粉、乳胶检查手套
K号: K161961 · 2017-05-11
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器械摘要
常见问题
What is the UniTex Non-Sterile, Powder-Free, Latex Examination Glove?
UniTex Non-Sterile, Powder-Free, Latex Examination Glove is a medical device that received FDA 510(k) clearance on 2017-05-11. The listed applicant is Ug Global Resources Sdn. Bhd.. The 510(k) number is K161961.
When did UniTex Non-Sterile, Powder-Free, Latex Examination Glove receive FDA 510(k) clearance?
UniTex Non-Sterile, Powder-Free, Latex Examination Glove received FDA 510(k) clearance on 2017-05-11, under 510(k) number K161961.
Who is the listed applicant for UniTex Non-Sterile, Powder-Free, Latex Examination Glove?
The FDA 510(k) record lists Ug Global Resources Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UniTex Non-Sterile, Powder-Free, Latex Examination Glove?
The FDA product code for UniTex Non-Sterile, Powder-Free, Latex Examination Glove is LYY.
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Ug Global Resources Sdn. Bhd.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:LYY)
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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