FDA 510(k)

mOm 精準培養箱 (ME1)

K 號：K243437 · 2025-08-14

決定日期2025-08-14

產品代碼FMZ

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

mOm Essential Incubator (ME1) is the device name listed in this FDA 510(k) record. The listed applicant is Mom Incubators Limited. It received FDA 510(k) clearance on 2025-08-14 under 510(k) number K243437. The device is classified under product code FMZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the mOm Essential Incubator (ME1)?

mOm Essential Incubator (ME1) is a medical device that received FDA 510(k) clearance on 2025-08-14. The listed applicant is Mom Incubators Limited. The 510(k) number is K243437.

When did mOm Essential Incubator (ME1) receive FDA 510(k) clearance?

mOm Essential Incubator (ME1) received FDA 510(k) clearance on 2025-08-14, under 510(k) number K243437.

Who is the listed applicant for mOm Essential Incubator (ME1)?

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

What is the FDA product code for mOm Essential Incubator (ME1)?

The FDA product code for mOm Essential Incubator (ME1) is FMZ.

相關器械（代碼：FMZ）

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官方來源

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：FMZ）

官方來源