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FDA 510(k)

Celerity 雾化 VH2O2 處理指示粘貼標籤 (PCC078)

K 號:K233187 · 2023-10-27

申請人Steris
決定日期2023-10-27
產品代碼JOJ
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

Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) is the device name listed in this FDA 510(k) record. The listed applicant is Steris. It received FDA 510(k) clearance on 2023-10-27 under 510(k) number K233187. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)?

Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) is a medical device that received FDA 510(k) clearance on 2023-10-27. The listed applicant is Steris. The 510(k) number is K233187.

When did Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) receive FDA 510(k) clearance?

Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) received FDA 510(k) clearance on 2023-10-27, under 510(k) number K233187.

Who is the listed applicant for Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)?

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

What is the FDA product code for Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)?

The FDA product code for Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) is JOJ.

相關臨床試驗

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其他以 Steris 為申請人之記錄

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相關器械(代碼:JOJ)

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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