FDA 510(k)

Tina-quant 血糖化血红蛋白 A1c Dx Gen.3

K 號：K193053 · 2020-03-26

決定日期2020-03-26

產品代碼PDJ

諮詢委員會CH

決定相當於

器材摘要

Tina-quant Hemoglobin A1cDx Gen.3 is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics Operations (Rdo). It received FDA 510(k) clearance on 2020-03-26 under 510(k) number K193053. The device is classified under product code PDJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tina-quant Hemoglobin A1cDx Gen.3?

Tina-quant Hemoglobin A1cDx Gen.3 is a medical device that received FDA 510(k) clearance on 2020-03-26. The listed applicant is Roche Diagnostics Operations (Rdo). The 510(k) number is K193053.

When did Tina-quant Hemoglobin A1cDx Gen.3 receive FDA 510(k) clearance?

Tina-quant Hemoglobin A1cDx Gen.3 received FDA 510(k) clearance on 2020-03-26, under 510(k) number K193053.

Who is the listed applicant for Tina-quant Hemoglobin A1cDx Gen.3?

The FDA 510(k) record lists Roche Diagnostics Operations (Rdo) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tina-quant Hemoglobin A1cDx Gen.3?

The FDA product code for Tina-quant Hemoglobin A1cDx Gen.3 is PDJ.

其他以 Roche Diagnostics Operations (Rdo) 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：PDJ）

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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