MR條件CGA 870
K 號：K162811 · 2017-03-02
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器材摘要
MR Conditional CGA 870 is the device name listed in this FDA 510(k) record. The listed applicant is Essex Industries, Inc.. It received FDA 510(k) clearance on 2017-03-02 under 510(k) number K162811. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MR Conditional CGA 870?
MR Conditional CGA 870 is a medical device that received FDA 510(k) clearance on 2017-03-02. The listed applicant is Essex Industries, Inc.. The 510(k) number is K162811.
When did MR Conditional CGA 870 receive FDA 510(k) clearance?
MR Conditional CGA 870 received FDA 510(k) clearance on 2017-03-02, under 510(k) number K162811.
Who is the listed applicant for MR Conditional CGA 870?
The FDA 510(k) record lists Essex Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MR Conditional CGA 870?
The FDA product code for MR Conditional CGA 870 is CAN.
相關臨床試驗
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其他以 Essex Industries, 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。
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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