AGENT，BULKING，注射用胃腸泌尿科用
PMA 核准號：P040050 · 2023-05-09
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器材摘要
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE is the device name listed in this FDA 510(k) record. The listed applicant is Uroplasty, LLC. It received FDA 510(k) clearance on 2023-05-09. The device is classified under product code LNM. It was reviewed by the GU advisory panel.
常見問題
What is the AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE?
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE is a medical device that received FDA 510(k) clearance on 2023-05-09. The listed applicant is Uroplasty, LLC.
When did AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE receive FDA 510(k) clearance?
The clearance date for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE can be found in the official FDA records.
Who is the listed applicant for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE?
The FDA 510(k) record lists Uroplasty, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE?
The FDA product code for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE is LNM.
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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