Erbe的CO2管/蓋組
K 號：K162152 · 2016-08-31
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器材摘要
Erbe’s CO2 Tubing/Cap Sets is the device name listed in this FDA 510(k) record. The listed applicant is Erbe USA, Inc.. It received FDA 510(k) clearance on 2016-08-31 under 510(k) number K162152. The device is classified under product code FEQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Erbe’s CO2 Tubing/Cap Sets?
Erbe’s CO2 Tubing/Cap Sets is a medical device that received FDA 510(k) clearance on 2016-08-31. The listed applicant is Erbe USA, Inc.. The 510(k) number is K162152.
When did Erbe’s CO2 Tubing/Cap Sets receive FDA 510(k) clearance?
Erbe’s CO2 Tubing/Cap Sets received FDA 510(k) clearance on 2016-08-31, under 510(k) number K162152.
Who is the listed applicant for Erbe’s CO2 Tubing/Cap Sets?
The FDA 510(k) record lists Erbe USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Erbe’s CO2 Tubing/Cap Sets?
The FDA product code for Erbe’s CO2 Tubing/Cap Sets is FEQ.
相關臨床試驗
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其他以 Erbe USA, Inc. 為申請人之記錄
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。
相關器械（代碼：FEQ）
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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