膠質繃帶
K 號：K172010 · 2017-12-07
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器材摘要
gel-e Bandage is the device name listed in this FDA 510(k) record. The listed applicant is Gel-E, Inc. (Formerly Remedium Technologies, Inc.). It received FDA 510(k) clearance on 2017-12-07 under 510(k) number K172010. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.
常見問題
What is the gel-e Bandage?
gel-e Bandage is a medical device that received FDA 510(k) clearance on 2017-12-07. The listed applicant is Gel-E, Inc. (Formerly Remedium Technologies, Inc.). The 510(k) number is K172010.
When did gel-e Bandage receive FDA 510(k) clearance?
gel-e Bandage received FDA 510(k) clearance on 2017-12-07, under 510(k) number K172010.
Who is the listed applicant for gel-e Bandage?
The FDA 510(k) record lists Gel-E, Inc. (Formerly Remedium Technologies, Inc.) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for gel-e Bandage?
The FDA product code for gel-e Bandage is KGN.
相關臨床試驗
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相關器械（代碼：KGN）
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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