ADMIRE
K号: K153360 · 2016-06-29
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器械摘要
ADMIRE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medi Cal Solutions, Inc.. It received FDA 510(k) clearance on 2016-06-29 under 510(k) number K153360. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ADMIRE?
ADMIRE is a medical device that received FDA 510(k) clearance on 2016-06-29. The listed applicant is Siemens Medi Cal Solutions, Inc.. The 510(k) number is K153360.
When did ADMIRE receive FDA 510(k) clearance?
ADMIRE received FDA 510(k) clearance on 2016-06-29, under 510(k) number K153360.
Who is the listed applicant for ADMIRE?
The FDA 510(k) record lists Siemens Medi Cal Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADMIRE?
The FDA product code for ADMIRE is JAK.
相关临床试验
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列明Siemens Medi Cal Solutions, Inc.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：JAK）
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。
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官方来源
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