CT6485, CT12885
K号: K172058 · 2018-02-13
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器械摘要
CT6485, CT12885 is the device name listed in this FDA 510(k) record. The listed applicant is Analogic Corporation. It received FDA 510(k) clearance on 2018-02-13 under 510(k) number K172058. 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 CT6485, CT12885?
CT6485, CT12885 is a medical device that received FDA 510(k) clearance on 2018-02-13. The listed applicant is Analogic Corporation. The 510(k) number is K172058.
When did CT6485, CT12885 receive FDA 510(k) clearance?
CT6485, CT12885 received FDA 510(k) clearance on 2018-02-13, under 510(k) number K172058.
Who is the listed applicant for CT6485, CT12885?
The FDA 510(k) record lists Analogic Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CT6485, CT12885?
The FDA product code for CT6485, CT12885 is JAK.
列明Analogic 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：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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