GEM
K 號：K213385 · 2022-07-01
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器材摘要
GEM is the device name listed in this FDA 510(k) record. The listed applicant is Obsidio, Inc.. It received FDA 510(k) clearance on 2022-07-01 under 510(k) number K213385. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the GEM?
GEM is a medical device that received FDA 510(k) clearance on 2022-07-01. The listed applicant is Obsidio, Inc.. The 510(k) number is K213385.
When did GEM receive FDA 510(k) clearance?
GEM received FDA 510(k) clearance on 2022-07-01, under 510(k) number K213385.
Who is the listed applicant for GEM?
The FDA 510(k) record lists Obsidio, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GEM?
The FDA product code for GEM is KRD.
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相關器械（代碼：KRD）
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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