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FDA 510(k)

Stryker 胸盾 消毒托盤系統

K 號:K183701 · 2019-05-07

決定日期2019-05-07
產品代碼KCT
諮詢委員會醫療設備規範文本翻譯如下: HO 注意:原文中未提供具體的醫療設備規範文本,因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於

器材摘要

Stryker ChestShield Sterilization Tray System is the device name listed in this FDA 510(k) record. The listed applicant is Paragon Medical. It received FDA 510(k) clearance on 2019-05-07 under 510(k) number K183701. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Stryker ChestShield Sterilization Tray System?

Stryker ChestShield Sterilization Tray System is a medical device that received FDA 510(k) clearance on 2019-05-07. The listed applicant is Paragon Medical. The 510(k) number is K183701.

When did Stryker ChestShield Sterilization Tray System receive FDA 510(k) clearance?

Stryker ChestShield Sterilization Tray System received FDA 510(k) clearance on 2019-05-07, under 510(k) number K183701.

Who is the listed applicant for Stryker ChestShield Sterilization Tray System?

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

What is the FDA product code for Stryker ChestShield Sterilization Tray System?

The FDA product code for Stryker ChestShield Sterilization Tray System is KCT.

相關臨床試驗

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其他以 Paragon Medical 為申請人之記錄

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相關器械(代碼:KCT)

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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