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FDA PMA

胎盤α微球蛋白-1免疫測定

PMA 核准號:P160052 · 2019-10-11

申請人Qiagen, Inc.
決定日期2019-10-11
PMA 編號P160052
產品代碼QBB
器械分類3 類
醫療專科U
諮詢委員會此醫療器材法規描述涉及FDA、510(k)、PMA、NCT、PMID及相關網址,以下為繁體中文翻譯: 本醫療器材之監管狀態係依據美國食品藥物管理局(FDA)之相關規定,包括510(k)上市前通知及PMA上市前核准程序。相關臨床試驗資訊可參閱NCT編號及PMID文獻編號,詳細資料請見所附網址。

器材摘要

Placental alpha microglobulin-1 immunoassay is the device name listed in this FDA 510(k) record. The listed applicant is Qiagen, Inc.. It received FDA 510(k) clearance on 2019-10-11. The device is classified under product code QBB. It was reviewed by the TX advisory panel.

常見問題

What is the Placental alpha microglobulin-1 immunoassay?

Placental alpha microglobulin-1 immunoassay is a medical device that received FDA 510(k) clearance on 2019-10-11. The listed applicant is Qiagen, Inc..

When did Placental alpha microglobulin-1 immunoassay receive FDA 510(k) clearance?

The clearance date for Placental alpha microglobulin-1 immunoassay can be found in the official FDA records.

Who is the listed applicant for Placental alpha microglobulin-1 immunoassay?

The FDA 510(k) record lists Qiagen, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Placental alpha microglobulin-1 immunoassay?

The FDA product code for Placental alpha microglobulin-1 immunoassay is QBB.

相關臨床試驗

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官方來源

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