AnemoCheck 家用版
K 號：K221508 · 2023-09-29
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器材摘要
AnemoCheck Home is the device name listed in this FDA 510(k) record. The listed applicant is Sanguina, Inc.. It received FDA 510(k) clearance on 2023-09-29 under 510(k) number K221508. The device is classified under product code KHG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the AnemoCheck Home?
AnemoCheck Home is a medical device that received FDA 510(k) clearance on 2023-09-29. The listed applicant is Sanguina, Inc.. The 510(k) number is K221508.
When did AnemoCheck Home receive FDA 510(k) clearance?
AnemoCheck Home received FDA 510(k) clearance on 2023-09-29, under 510(k) number K221508.
Who is the listed applicant for AnemoCheck Home?
The FDA 510(k) record lists Sanguina, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AnemoCheck Home?
The FDA product code for AnemoCheck Home is KHG.
相關臨床試驗
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相關器械（代碼：KHG）
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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