Medipoint 體液針
K 號：K223480 · 2023-01-13
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器材摘要
Medipoint Blood Lancets is the device name listed in this FDA 510(k) record. The listed applicant is Medipoint Holdings, LLC. It received FDA 510(k) clearance on 2023-01-13 under 510(k) number K223480. The device is classified under product code QRK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Medipoint Blood Lancets?
Medipoint Blood Lancets is a medical device that received FDA 510(k) clearance on 2023-01-13. The listed applicant is Medipoint Holdings, LLC. The 510(k) number is K223480.
When did Medipoint Blood Lancets receive FDA 510(k) clearance?
Medipoint Blood Lancets received FDA 510(k) clearance on 2023-01-13, under 510(k) number K223480.
Who is the listed applicant for Medipoint Blood Lancets?
The FDA 510(k) record lists Medipoint Holdings, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medipoint Blood Lancets?
The FDA product code for Medipoint Blood Lancets is QRK.
相關臨床試驗
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相關器械（代碼：QRK）
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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