Kidro数字电动吸奶器,Dr. Brown的数字电动吸奶器
K号: K192640 · 2020-03-30
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器械摘要
常见问题
What is the Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump?
Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump is a medical device that received FDA 510(k) clearance on 2020-03-30. The listed applicant is Guangzhou Yongyi Industrial Co., Ltd.. The 510(k) number is K192640.
When did Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump receive FDA 510(k) clearance?
Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump received FDA 510(k) clearance on 2020-03-30, under 510(k) number K192640.
Who is the listed applicant for Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump?
The FDA 510(k) record lists Guangzhou Yongyi Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump?
The FDA product code for Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump is HGX.
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Guangzhou Yongyi Industrial 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:HGX)
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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