FDA 510(k)

Aimanfun Lumea Comfort, 型號：A-2788, A-2789和A-3588

K 號：K230107 · 2023-04-05

決定日期2023-04-05

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

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 is the device name listed in this FDA 510(k) record. The listed applicant is Kam Yuen Plastic Products , Ltd.. It received FDA 510(k) clearance on 2023-04-05 under 510(k) number K230107. 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 Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588?

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 is a medical device that received FDA 510(k) clearance on 2023-04-05. The listed applicant is Kam Yuen Plastic Products , Ltd.. The 510(k) number is K230107.

When did Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 receive FDA 510(k) clearance?

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 received FDA 510(k) clearance on 2023-04-05, under 510(k) number K230107.

Who is the listed applicant for Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588?

FDA 510(k) 記錄將高圓塑料產品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 Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588?

The FDA product code for Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 is OHT.

其他以 Kam Yuen Plastic Products , 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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