水濕化器
K 號：K201740 · 2021-07-07
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器材摘要
Hydrozid is the device name listed in this FDA 510(k) record. The listed applicant is Medilink A/S. It received FDA 510(k) clearance on 2021-07-07 under 510(k) number K201740. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Hydrozid?
Hydrozid is a medical device that received FDA 510(k) clearance on 2021-07-07. The listed applicant is Medilink A/S. The 510(k) number is K201740.
When did Hydrozid receive FDA 510(k) clearance?
Hydrozid received FDA 510(k) clearance on 2021-07-07, under 510(k) number K201740.
Who is the listed applicant for Hydrozid?
The FDA 510(k) record lists Medilink A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hydrozid?
The FDA product code for Hydrozid is GEH.
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相關器械（代碼：GEH）
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
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