EasyScreen 消化道寄生蟲檢測套件
K 號：K232672 · 2024-05-29
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器材摘要
EasyScreen Gastrointestinal Parasite Detection Kit is the device name listed in this FDA 510(k) record. The listed applicant is Genetic Signatures Limited. It received FDA 510(k) clearance on 2024-05-29 under 510(k) number K232672. The device is classified under product code PCH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the EasyScreen Gastrointestinal Parasite Detection Kit?
EasyScreen Gastrointestinal Parasite Detection Kit is a medical device that received FDA 510(k) clearance on 2024-05-29. The listed applicant is Genetic Signatures Limited. The 510(k) number is K232672.
When did EasyScreen Gastrointestinal Parasite Detection Kit receive FDA 510(k) clearance?
EasyScreen Gastrointestinal Parasite Detection Kit received FDA 510(k) clearance on 2024-05-29, under 510(k) number K232672.
Who is the listed applicant for EasyScreen Gastrointestinal Parasite Detection Kit?
The FDA 510(k) record lists Genetic Signatures Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EasyScreen Gastrointestinal Parasite Detection Kit?
The FDA product code for EasyScreen Gastrointestinal Parasite Detection Kit is PCH.
相關臨床試驗
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相關器械（代碼：PCH）
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
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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