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FDA 510(k)

芬尼斯強力聚異戊二烯外科手套

K 號:K173304 · 2018-04-30

決定日期2018-04-30
產品代碼KGO
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

Finessis Intense Polyisoprene Surgical Glove is the device name listed in this FDA 510(k) record. The listed applicant is Lucenxia Prescience AG. It received FDA 510(k) clearance on 2018-04-30 under 510(k) number K173304. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Finessis Intense Polyisoprene Surgical Glove?

Finessis Intense Polyisoprene Surgical Glove is a medical device that received FDA 510(k) clearance on 2018-04-30. The listed applicant is Lucenxia Prescience AG. The 510(k) number is K173304.

When did Finessis Intense Polyisoprene Surgical Glove receive FDA 510(k) clearance?

Finessis Intense Polyisoprene Surgical Glove received FDA 510(k) clearance on 2018-04-30, under 510(k) number K173304.

Who is the listed applicant for Finessis Intense Polyisoprene Surgical Glove?

The FDA 510(k) record lists Lucenxia Prescience AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Finessis Intense Polyisoprene Surgical Glove?

The FDA product code for Finessis Intense Polyisoprene Surgical Glove is KGO.

相關臨床試驗

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其他以 Lucenxia Prescience AG 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:KGO)

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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