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FDA 510(k)

iFlash-HCG;化學發光免疫分析儀(型號:iFlash 3000-C)

K 號:K223690 · 2023-12-11

決定日期2023-12-11
產品代碼DHA
諮詢委員會CH
決定相當於

器材摘要

iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Yhlo Biotech Co., Ltd.. It received FDA 510(k) clearance on 2023-12-11 under 510(k) number K223690. The device is classified under product code DHA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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

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