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FDA 510(k)

醫療設備名稱:Medicell Mycosis Laser (MCML24004)

K 號:K253960 · 2026-03-09

決定日期2026-03-09
產品代碼PDZ
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

Medicell Mycosis Laser (MCML24004) is the device name listed in this FDA 510(k) record. The listed applicant is Medicell Healthcare Co.,LTD. It received FDA 510(k) clearance on 2026-03-09 under 510(k) number K253960. The device is classified under product code PDZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Medicell Mycosis Laser (MCML24004)?

Medicell Mycosis Laser (MCML24004) is a medical device that received FDA 510(k) clearance on 2026-03-09. The listed applicant is Medicell Healthcare Co.,LTD. The 510(k) number is K253960.

When did Medicell Mycosis Laser (MCML24004) receive FDA 510(k) clearance?

Medicell Mycosis Laser (MCML24004) received FDA 510(k) clearance on 2026-03-09, under 510(k) number K253960.

Who is the listed applicant for Medicell Mycosis Laser (MCML24004)?

The FDA 510(k) record lists Medicell Healthcare Co.,LTD as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medicell Mycosis Laser (MCML24004)?

The FDA product code for Medicell Mycosis Laser (MCML24004) is PDZ.

相關臨床試驗

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相關器械(代碼:PDZ)

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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