LATEX 检查手套 无粉
K号: K152593 · 2016-02-25
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器械摘要
常见问题
What is the LATEX EXAMINATION GLOVE POWDER FREE?
LATEX EXAMINATION GLOVE POWDER FREE is a medical device that received FDA 510(k) clearance on 2016-02-25. The listed applicant is Careplus (M) Sdn Bhd. The 510(k) number is K152593.
When did LATEX EXAMINATION GLOVE POWDER FREE receive FDA 510(k) clearance?
LATEX EXAMINATION GLOVE POWDER FREE received FDA 510(k) clearance on 2016-02-25, under 510(k) number K152593.
Who is the listed applicant for LATEX EXAMINATION GLOVE POWDER FREE?
The FDA 510(k) record lists Careplus (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAMINATION GLOVE POWDER FREE?
The FDA product code for LATEX EXAMINATION GLOVE POWDER FREE 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Careplus (M) 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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