FDA 510(k)

cobas Influenza A/B & RSV 鈾酸測試，適用於 cobas Liat 系統

K 號：K210234 · 2021-02-16

決定日期2021-02-16

產品代碼OCC

諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)

決定相當於

器材摘要

cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System is the device name listed in this FDA 510(k) record. The listed applicant is Roche Molecular Systems, Inc.. It received FDA 510(k) clearance on 2021-02-16 under 510(k) number K210234. The device is classified under product code OCC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System?

cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System is a medical device that received FDA 510(k) clearance on 2021-02-16. The listed applicant is Roche Molecular Systems, Inc.. The 510(k) number is K210234.

When did cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System receive FDA 510(k) clearance?

cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System received FDA 510(k) clearance on 2021-02-16, under 510(k) number K210234.

Who is the listed applicant for cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System?

FDA 510(k) 記錄將羅氏分子系統公司（Roche Molecular Systems, 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 cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System?

The FDA product code for cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System is OCC.

其他以 Roche Molecular Systems, Inc. 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。

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相關器械（代碼：OCC）

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

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