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FDA 510(k)

Unico Global 第三級手術袍(膠膜強化SMS),Unico Global 第三級手術袍(PP+PE)

K 號:K203539 · 2021-12-10

決定日期2021-12-10
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

Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE) is the device name listed in this FDA 510(k) record. The listed applicant is Unicoglobal, Inc.. It received FDA 510(k) clearance on 2021-12-10 under 510(k) number K203539. 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 Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE)?

Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE) is a medical device that received FDA 510(k) clearance on 2021-12-10. The listed applicant is Unicoglobal, Inc.. The 510(k) number is K203539.

When did Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE) receive FDA 510(k) clearance?

Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE) received FDA 510(k) clearance on 2021-12-10, under 510(k) number K203539.

Who is the listed applicant for Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE)?

The FDA 510(k) record lists Unicoglobal, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE)?

The FDA product code for Unico Global level 3 Surgical Gown (Film-reinforced SMS), Unico Global Level 3 Surgical Gown (PP+PE) is FYA.

相關臨床試驗

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其他以 Unicoglobal, 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: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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