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FDA 510(k)

GentleCath Air 女性用 (CH10);GentleCath Air 女性用 (CH12);GentleCath Air 女性用 (CH14)

K 號:K232665 · 2024-01-25

申請人Convatec
決定日期2024-01-25
產品代碼EZD
諮詢委員會GU
決定相當於

器材摘要

GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14) is the device name listed in this FDA 510(k) record. The listed applicant is Convatec. It received FDA 510(k) clearance on 2024-01-25 under 510(k) number K232665. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14)?

GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14) is a medical device that received FDA 510(k) clearance on 2024-01-25. The listed applicant is Convatec. The 510(k) number is K232665.

When did GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14) receive FDA 510(k) clearance?

GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14) received FDA 510(k) clearance on 2024-01-25, under 510(k) number K232665.

Who is the listed applicant for GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14)?

FDA 510(k) 記錄將 Convatec 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14)?

The FDA product code for GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14) is EZD.

相關臨床試驗

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。

其他以 Convatec 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:EZD)

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

在 FDA 資料庫中查看 →

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