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FDA 510(k)

Alinity c ICT樣本稀釋劑

K 號:K170320 · 2017-10-24

決定日期2017-10-24
產品代碼CGZ
諮詢委員會CH
決定相當於

器材摘要

Alinity c ICT Sample Diluent is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2017-10-24 under 510(k) number K170320. The device is classified under product code CGZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Alinity c ICT Sample Diluent?

Alinity c ICT Sample Diluent is a medical device that received FDA 510(k) clearance on 2017-10-24. The listed applicant is Abbott Laboratories. The 510(k) number is K170320.

When did Alinity c ICT Sample Diluent receive FDA 510(k) clearance?

Alinity c ICT Sample Diluent received FDA 510(k) clearance on 2017-10-24, under 510(k) number K170320.

Who is the listed applicant for Alinity c ICT Sample Diluent?

FDA 510(k) 記錄中將阿培爾實驗室列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Alinity c ICT Sample Diluent?

The FDA product code for Alinity c ICT Sample Diluent is CGZ.

相關臨床試驗

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其他以 Abbott Laboratories 為申請人之記錄

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相關器械(代碼:CGZ)

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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