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FDA 510(k)

舒適保護外科袍,i600,膠片加固

K 號:K163191 · 2017-02-27

決定日期2017-02-27
產品代碼FYA
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

ComfortGuard Surgical Gown, i600, Film Reinforced is the device name listed in this FDA 510(k) record. The listed applicant is Gri Medical & Electrical Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-02-27 under 510(k) number K163191. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ComfortGuard Surgical Gown, i600, Film Reinforced?

ComfortGuard Surgical Gown, i600, Film Reinforced is a medical device that received FDA 510(k) clearance on 2017-02-27. The listed applicant is Gri Medical & Electrical Technology Co., Ltd.. The 510(k) number is K163191.

When did ComfortGuard Surgical Gown, i600, Film Reinforced receive FDA 510(k) clearance?

ComfortGuard Surgical Gown, i600, Film Reinforced received FDA 510(k) clearance on 2017-02-27, under 510(k) number K163191.

Who is the listed applicant for ComfortGuard Surgical Gown, i600, Film Reinforced?

The FDA 510(k) record lists Gri Medical & Electrical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ComfortGuard Surgical Gown, i600, Film Reinforced?

The FDA product code for ComfortGuard Surgical Gown, i600, Film Reinforced is FYA.

相關臨床試驗

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其他以 Gri Medical & Electrical Technology Co., Ltd. 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:FYA)

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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