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FDA 510(k)

Applied Biosystems™ 3500 Dx 遺傳分析儀和Applied Biosystems™ 3500xL Dx 遺傳分析儀

K 號：K191030 · 2020-02-21

申請人Life Technologies Corporation
決定日期2020-02-21
產品代碼PCA
諮詢委員會CH
決定相當於

器材摘要

Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer is the device name listed in this FDA 510(k) record. The listed applicant is Life Technologies Corporation. It received FDA 510(k) clearance on 2020-02-21 under 510(k) number K191030. The device is classified under product code PCA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer?

Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer is a medical device that received FDA 510(k) clearance on 2020-02-21. The listed applicant is Life Technologies Corporation. The 510(k) number is K191030.

When did Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer receive FDA 510(k) clearance?

Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer received FDA 510(k) clearance on 2020-02-21, under 510(k) number K191030.

Who is the listed applicant for Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer?

The FDA 510(k) record lists Life Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer?

The FDA product code for Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer is PCA.

相關臨床試驗

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NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

其他以 Life Technologies Corporation 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。

K241806Applied Biosystems™ TaqPath™ COVID-19、流感A、流感B、RSV選擇面板K233453Applied Biosystems™ TaqPath™ COVID-19 诊断PCR試劑套件K170299離子PGM Dx系統

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