iFlash-HCG;化學發光免疫分析儀(型號:iFlash 3000-C)
K 號:K223690 · 2023-12-11
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器材摘要
常見問題
What is the iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C)?
iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C) is a medical device that received FDA 510(k) clearance on 2023-12-11. The listed applicant is Shenzhen Yhlo Biotech Co., Ltd.. The 510(k) number is K223690.
When did iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C) receive FDA 510(k) clearance?
iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C) received FDA 510(k) clearance on 2023-12-11, under 510(k) number K223690.
Who is the listed applicant for iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C)?
The FDA 510(k) record lists Shenzhen Yhlo Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C)?
The FDA product code for iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C) is DHA.
相關臨床試驗
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相關器械(代碼:DHA)
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。
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