FDA 510(k)

“FLNT 基座”及“FLNT 溫度”

K 號：K253380 · 2026-03-02

決定日期2026-03-02

產品代碼EBG

諮詢委員會DE

決定相當於

器材摘要

“FLNT Base” and “FLNT Temp” is the device name listed in this FDA 510(k) record. The listed applicant is Liaoning Upcera Co., Ltd.. It received FDA 510(k) clearance on 2026-03-02 under 510(k) number K253380. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the “FLNT Base” and “FLNT Temp”?

“FLNT Base” and “FLNT Temp” is a medical device that received FDA 510(k) clearance on 2026-03-02. The listed applicant is Liaoning Upcera Co., Ltd.. The 510(k) number is K253380.

When did “FLNT Base” and “FLNT Temp” receive FDA 510(k) clearance?

“FLNT Base” and “FLNT Temp” received FDA 510(k) clearance on 2026-03-02, under 510(k) number K253380.

Who is the listed applicant for “FLNT Base” and “FLNT Temp”?

The FDA 510(k) record lists Liaoning Upcera Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for “FLNT Base” and “FLNT Temp”?

The FDA product code for “FLNT Base” and “FLNT Temp” is EBG.

其他以 Liaoning Upcera Co., Ltd. 為申請人之記錄

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相關器械（代碼：EBG）

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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