海神籠
K 號：K183407 · 2019-08-30
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器材摘要
Triton Cage is the device name listed in this FDA 510(k) record. The listed applicant is Medyssey USA, Inc.. It received FDA 510(k) clearance on 2019-08-30 under 510(k) number K183407. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Triton Cage?
Triton Cage is a medical device that received FDA 510(k) clearance on 2019-08-30. The listed applicant is Medyssey USA, Inc.. The 510(k) number is K183407.
When did Triton Cage receive FDA 510(k) clearance?
Triton Cage received FDA 510(k) clearance on 2019-08-30, under 510(k) number K183407.
Who is the listed applicant for Triton Cage?
The FDA 510(k) record lists Medyssey USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Triton Cage?
The FDA product code for Triton Cage is MAX.
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其他以 Medyssey 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：MAX）
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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