1Derful HS, 1Derful HT
K 號：K210884 · 2021-07-27
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器材摘要
1Derful HS, 1Derful HT is the device name listed in this FDA 510(k) record. The listed applicant is 1derful, Inc.. It received FDA 510(k) clearance on 2021-07-27 under 510(k) number K210884. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the 1Derful HS, 1Derful HT?
1Derful HS, 1Derful HT is a medical device that received FDA 510(k) clearance on 2021-07-27. The listed applicant is 1derful, Inc.. The 510(k) number is K210884.
When did 1Derful HS, 1Derful HT receive FDA 510(k) clearance?
1Derful HS, 1Derful HT received FDA 510(k) clearance on 2021-07-27, under 510(k) number K210884.
Who is the listed applicant for 1Derful HS, 1Derful HT?
The FDA 510(k) record lists 1derful, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1Derful HS, 1Derful HT?
The FDA product code for 1Derful HS, 1Derful HT is EIH.
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相關器械（代碼：EIH）
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
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