安全針筒
K 號：K222801 · 2023-01-25
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器材摘要
Safety Lancet is the device name listed in this FDA 510(k) record. The listed applicant is Sarstedt AG & CO KG. It received FDA 510(k) clearance on 2023-01-25 under 510(k) number K222801. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Safety Lancet?
Safety Lancet is a medical device that received FDA 510(k) clearance on 2023-01-25. The listed applicant is Sarstedt AG & CO KG. The 510(k) number is K222801.
When did Safety Lancet receive FDA 510(k) clearance?
Safety Lancet received FDA 510(k) clearance on 2023-01-25, under 510(k) number K222801.
Who is the listed applicant for Safety Lancet?
The FDA 510(k) record lists Sarstedt AG & CO KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Safety Lancet?
The FDA product code for Safety Lancet is FMK.
相關臨床試驗
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相關器械（代碼：FMK）
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。
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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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