SpeqT
K号: K160420 · 2016-03-21
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器械摘要
SpeqT is the device name listed in this FDA 510(k) record. The listed applicant is Signostics Limited. It received FDA 510(k) clearance on 2016-03-21 under 510(k) number K160420. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SpeqT?
SpeqT is a medical device that received FDA 510(k) clearance on 2016-03-21. The listed applicant is Signostics Limited. The 510(k) number is K160420.
When did SpeqT receive FDA 510(k) clearance?
SpeqT received FDA 510(k) clearance on 2016-03-21, under 510(k) number K160420.
Who is the listed applicant for SpeqT?
The FDA 510(k) record lists Signostics Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SpeqT?
The FDA product code for SpeqT is IYO.
相关临床试验
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相关器械（代码：IYO）
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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