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FDA 510(k)

ACTICOAT 外科敷料

K 號:K153723 · 2016-09-14

決定日期2016-09-14
產品代碼FRO
決定相當於

器材摘要

ACTICOAT Surgical Dressing is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Medical Limited. It received FDA 510(k) clearance on 2016-09-14 under 510(k) number K153723. 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 ACTICOAT Surgical Dressing?

ACTICOAT Surgical Dressing is a medical device that received FDA 510(k) clearance on 2016-09-14. The listed applicant is Smith & Nephew Medical Limited. The 510(k) number is K153723.

When did ACTICOAT Surgical Dressing receive FDA 510(k) clearance?

ACTICOAT Surgical Dressing received FDA 510(k) clearance on 2016-09-14, under 510(k) number K153723.

Who is the listed applicant for ACTICOAT Surgical Dressing?

The FDA 510(k) record lists Smith & Nephew Medical Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTICOAT Surgical Dressing?

The FDA product code for ACTICOAT Surgical Dressing is FRO. This falls under the Anesthesiology category.

相關臨床試驗

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其他以 Smith & Nephew Medical Limited 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

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