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FDA 510(k)

AccessTSH(第3個IS)測試,DxI 9000Access免疫測定分析儀

K 號:K221225 · 2022-11-10

決定日期2022-11-10
產品代碼JLW
諮詢委員會CH
決定相當於

器材摘要

Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Coulter, Inc.. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K221225. The device is classified under product code JLW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer?

Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Beckman Coulter, Inc.. The 510(k) number is K221225.

When did Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer receive FDA 510(k) clearance?

Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer received FDA 510(k) clearance on 2022-11-10, under 510(k) number K221225.

Who is the listed applicant for Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer?

FDA 510(k) 記錄將 Beckman Coulter, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer?

The FDA product code for Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer is JLW.

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其他以 Beckman Coulter, Inc. 為申請人之記錄

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相關器械(代碼:JLW)

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官方來源

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