LIA Pregnancy Test
K号: K171136 · 2017-11-20
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决定日期2017-11-20
产品代码LCX
咨询委员会CH
请注意，您提供的文本“CH”不足以进行翻译。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
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器械摘要
LIA Pregnancy Test is the device name listed in this FDA 510(k) record. The listed applicant is Lia Diagnostics. It received FDA 510(k) clearance on 2017-11-20 under 510(k) number K171136. The device is classified under product code LCX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LIA Pregnancy Test?
LIA Pregnancy Test is a medical device that received FDA 510(k) clearance on 2017-11-20. The listed applicant is Lia Diagnostics. The 510(k) number is K171136.
When did LIA Pregnancy Test receive FDA 510(k) clearance?
LIA Pregnancy Test received FDA 510(k) clearance on 2017-11-20, under 510(k) number K171136.
Who is the listed applicant for LIA Pregnancy Test?
The FDA 510(k) record lists Lia Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIA Pregnancy Test?
The FDA product code for LIA Pregnancy Test is LCX.
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相关器械（代码：LCX）
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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