FDA 510(k)

手持式除毛設備（FZ-200A、FZ-201、FZ-202、CT05、CT06、CT07、CT08、CT09）

K 號：K251000 · 2025-06-30

申請人Shenzhen Chuangtong Yigou Technology Co., Ltd.

決定日期2025-06-30

產品代碼OHT

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

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Chuangtong Yigou Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-06-30 under 510(k) number K251000. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)?

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) is a medical device that received FDA 510(k) clearance on 2025-06-30. The listed applicant is Shenzhen Chuangtong Yigou Technology Co., Ltd.. The 510(k) number is K251000.

When did Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) receive FDA 510(k) clearance?

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) received FDA 510(k) clearance on 2025-06-30, under 510(k) number K251000.

Who is the listed applicant for Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)?

FDA 510(k) 記錄將深圳創通易購科技有限公司列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)?

The FDA product code for Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) is OHT.

其他以 Shenzhen Chuangtong Yigou Technology Co., Ltd. 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。

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相關器械（代碼：OHT）

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。

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官方來源

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