Exufiber Ag+
K 號：K160379 · 2016-08-25
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器材摘要
Exufiber Ag+ is the device name listed in this FDA 510(k) record. The listed applicant is Molnlycke Health Care Us, LLC. It received FDA 510(k) clearance on 2016-08-25 under 510(k) number K160379. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常見問題
What is the Exufiber Ag+?
Exufiber Ag+ is a medical device that received FDA 510(k) clearance on 2016-08-25. The listed applicant is Molnlycke Health Care Us, LLC. The 510(k) number is K160379.
When did Exufiber Ag+ receive FDA 510(k) clearance?
Exufiber Ag+ received FDA 510(k) clearance on 2016-08-25, under 510(k) number K160379.
Who is the listed applicant for Exufiber Ag+?
The FDA 510(k) record lists Molnlycke Health Care Us, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Exufiber Ag+?
The FDA product code for Exufiber Ag+ is FRO. This falls under the Anesthesiology category.
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其他以 Molnlycke Health Care Us, LLC 為申請人之記錄
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相關器械（代碼：FRO）
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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