iMedium 单步;iMedium 单步带HSA;iMedium 单步带rHA
K号: K193522 · 2020-08-25
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器械摘要
常见问题
What is the iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA?
iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA is a medical device that received FDA 510(k) clearance on 2020-08-25. The listed applicant is Kitazato Corporation. The 510(k) number is K193522.
When did iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA receive FDA 510(k) clearance?
iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA received FDA 510(k) clearance on 2020-08-25, under 510(k) number K193522.
Who is the listed applicant for iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA?
The FDA 510(k) record lists Kitazato Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA?
The FDA product code for iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA is MQL.
相关临床试验
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列明Kitazato Corporation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:MQL)
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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