維托斯輕量設備套件（MDK-0002）
K 號：K233800 · 2024-05-06
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器材摘要
Vertos mild Device Kit (MDK-0002) is the device name listed in this FDA 510(k) record. The listed applicant is Vertos Medical, Inc.. It received FDA 510(k) clearance on 2024-05-06 under 510(k) number K233800. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vertos mild Device Kit (MDK-0002)?
Vertos mild Device Kit (MDK-0002) is a medical device that received FDA 510(k) clearance on 2024-05-06. The listed applicant is Vertos Medical, Inc.. The 510(k) number is K233800.
When did Vertos mild Device Kit (MDK-0002) receive FDA 510(k) clearance?
Vertos mild Device Kit (MDK-0002) received FDA 510(k) clearance on 2024-05-06, under 510(k) number K233800.
Who is the listed applicant for Vertos mild Device Kit (MDK-0002)?
The FDA 510(k) record lists Vertos Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vertos mild Device Kit (MDK-0002)?
The FDA product code for Vertos mild Device Kit (MDK-0002) is HRX.
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相關器械（代碼：HRX）
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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