檢測腺病毒病毒載體（AAV）預存抗體的試劑
PMA 核准號：P250002 · 2025-07-24
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器材摘要
常見問題
What is the Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors?
Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors is a medical device that received FDA 510(k) clearance on 2025-07-24. The listed applicant is Quest Diagnostics Nichols Institute.
When did Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors receive FDA 510(k) clearance?
The clearance date for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors can be found in the official FDA records.
Who is the listed applicant for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors?
The FDA 510(k) record lists Quest Diagnostics Nichols Institute as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors?
The FDA product code for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors is QWQ.
相關臨床試驗
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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