羅盤可調針針與適配器 SRA-1-01 及 SRA-2-01
K 號:K252874 · 2025-10-08
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器材摘要
常見問題
What is the Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01?
Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01 is a medical device that received FDA 510(k) clearance on 2025-10-08. The listed applicant is Serpex Medical, Inc.. The 510(k) number is K252874.
When did Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01 receive FDA 510(k) clearance?
Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01 received FDA 510(k) clearance on 2025-10-08, under 510(k) number K252874.
Who is the listed applicant for Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01?
The FDA 510(k) record lists Serpex Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01?
The FDA product code for Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01 is KTI.
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。
其他以 Serpex Medical, Inc. 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。
相關器械(代碼:KTI)
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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