HemosIL 纤维蛋白原-C；HemosIL 纤维蛋白原-C XL
K 號：K251968 · 2025-07-24
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器材摘要
HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory (IL) Co.. It received FDA 510(k) clearance on 2025-07-24 under 510(k) number K251968. The device is classified under product code KQJ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL?
HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL is a medical device that received FDA 510(k) clearance on 2025-07-24. The listed applicant is Instrumentation Laboratory (IL) Co.. The 510(k) number is K251968.
When did HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL receive FDA 510(k) clearance?
HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL received FDA 510(k) clearance on 2025-07-24, under 510(k) number K251968.
Who is the listed applicant for HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL?
The FDA 510(k) record lists Instrumentation Laboratory (IL) Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL?
The FDA product code for HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL is KQJ.
相關臨床試驗
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其他以 Instrumentation Laboratory (IL) Co. 為申請人之記錄
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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