支架，尿道，前列腺，半永久性
PMA 核准號：P060010 · 2022-10-07
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器材摘要
Stent, urethral, prostatic, semi-permanent is the device name listed in this FDA 510(k) record. The listed applicant is Srs Medical. It received FDA 510(k) clearance on 2022-10-07. The device is classified under product code NZC. It was reviewed by the GU advisory panel.
常見問題
What is the Stent, urethral, prostatic, semi-permanent?
Stent, urethral, prostatic, semi-permanent is a medical device that received FDA 510(k) clearance on 2022-10-07. The listed applicant is Srs Medical.
When did Stent, urethral, prostatic, semi-permanent receive FDA 510(k) clearance?
The clearance date for Stent, urethral, prostatic, semi-permanent can be found in the official FDA records.
Who is the listed applicant for Stent, urethral, prostatic, semi-permanent?
The FDA 510(k) record lists Srs Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stent, urethral, prostatic, semi-permanent?
The FDA product code for Stent, urethral, prostatic, semi-permanent is NZC.
相關臨床試驗
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
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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