LIA懷孕檢測
K 號：K171136 · 2017-11-20
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器材摘要
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.
常見問題
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.
相關臨床試驗
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相關器械（代碼：LCX）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
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