MAGLUMI 2000 HCG/ß-HCG
K号: K192547 · 2020-01-17
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器械摘要
常见问题
What is the MAGLUMI 2000 HCG/ß-HCG?
MAGLUMI 2000 HCG/ß-HCG is a medical device that received FDA 510(k) clearance on 2020-01-17. The listed applicant is Shenzhen New Industries Biomedical Engineering Co., Ltd.. The 510(k) number is K192547.
When did MAGLUMI 2000 HCG/ß-HCG receive FDA 510(k) clearance?
MAGLUMI 2000 HCG/ß-HCG received FDA 510(k) clearance on 2020-01-17, under 510(k) number K192547.
Who is the listed applicant for MAGLUMI 2000 HCG/ß-HCG?
The FDA 510(k) record lists Shenzhen New Industries Biomedical Engineering Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAGLUMI 2000 HCG/ß-HCG?
The FDA product code for MAGLUMI 2000 HCG/ß-HCG is DHA.
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Shenzhen New Industries Biomedical Engineering Co., Ltd.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:DHA)
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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