非无菌无粉乳胶检查手套
K号: K221667 · 2022-10-28
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器械摘要
常见问题
What is the Non Sterile Powder Free Latex Examination Glove?
Non Sterile Powder Free Latex Examination Glove is a medical device that received FDA 510(k) clearance on 2022-10-28. The listed applicant is New Era Medicare Sdn. Bhd.. The 510(k) number is K221667.
When did Non Sterile Powder Free Latex Examination Glove receive FDA 510(k) clearance?
Non Sterile Powder Free Latex Examination Glove received FDA 510(k) clearance on 2022-10-28, under 510(k) number K221667.
Who is the listed applicant for Non Sterile Powder Free Latex Examination Glove?
The FDA 510(k) record lists New Era Medicare Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Non Sterile Powder Free Latex Examination Glove?
The FDA product code for 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New Era Medicare 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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