SurgiLance® 安全針頭
K 號：K222224 · 2022-09-22
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器材摘要
SurgiLance® Safety Lancet is the device name listed in this FDA 510(k) record. The listed applicant is Medipurpose Pte. , Ltd.. It received FDA 510(k) clearance on 2022-09-22 under 510(k) number K222224. 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 SurgiLance® Safety Lancet?
SurgiLance® Safety Lancet is a medical device that received FDA 510(k) clearance on 2022-09-22. The listed applicant is Medipurpose Pte. , Ltd.. The 510(k) number is K222224.
When did SurgiLance® Safety Lancet receive FDA 510(k) clearance?
SurgiLance® Safety Lancet received FDA 510(k) clearance on 2022-09-22, under 510(k) number K222224.
Who is the listed applicant for SurgiLance® Safety Lancet?
The FDA 510(k) record lists Medipurpose Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SurgiLance® Safety Lancet?
The FDA product code for SurgiLance® 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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