注射針（KIP(02031-02061) (03031-03061)）
K 號：K221697 · 2023-03-03
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器材摘要
INJECTION PIN (KIP(02031-02061) (03031-03061)) is the device name listed in this FDA 510(k) record. The listed applicant is Slk Ortho, LLC. It received FDA 510(k) clearance on 2023-03-03 under 510(k) number K221697. The device is classified under product code NDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the INJECTION PIN (KIP(02031-02061) (03031-03061))?
INJECTION PIN (KIP(02031-02061) (03031-03061)) is a medical device that received FDA 510(k) clearance on 2023-03-03. The listed applicant is Slk Ortho, LLC. The 510(k) number is K221697.
When did INJECTION PIN (KIP(02031-02061) (03031-03061)) receive FDA 510(k) clearance?
INJECTION PIN (KIP(02031-02061) (03031-03061)) received FDA 510(k) clearance on 2023-03-03, under 510(k) number K221697.
Who is the listed applicant for INJECTION PIN (KIP(02031-02061) (03031-03061))?
The FDA 510(k) record lists Slk Ortho, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INJECTION PIN (KIP(02031-02061) (03031-03061))?
The FDA product code for INJECTION PIN (KIP(02031-02061) (03031-03061)) is NDN.
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。
相關器械（代碼：NDN）
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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