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FDA 510(k)

Tandem Mobi 胰島素針筒配互操作性技術

K 號:K253074 · 2025-11-06

決定日期2025-11-06
產品代碼QFG
諮詢委員會CH
決定相當於

器材摘要

Tandem Mobi insulin pump with interoperable technology is the device name listed in this FDA 510(k) record. The listed applicant is Tandem Diabetes Care, Inc.. It received FDA 510(k) clearance on 2025-11-06 under 510(k) number K253074. The device is classified under product code QFG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tandem Mobi insulin pump with interoperable technology?

Tandem Mobi insulin pump with interoperable technology is a medical device that received FDA 510(k) clearance on 2025-11-06. The listed applicant is Tandem Diabetes Care, Inc.. The 510(k) number is K253074.

When did Tandem Mobi insulin pump with interoperable technology receive FDA 510(k) clearance?

Tandem Mobi insulin pump with interoperable technology received FDA 510(k) clearance on 2025-11-06, under 510(k) number K253074.

Who is the listed applicant for Tandem Mobi insulin pump with interoperable technology?

The FDA 510(k) record lists Tandem Diabetes Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tandem Mobi insulin pump with interoperable technology?

The FDA product code for Tandem Mobi insulin pump with interoperable technology is QFG.

相關臨床試驗

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其他以 Tandem Diabetes Care, Inc. 為申請人之記錄

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相關器械(代碼:QFG)

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官方來源

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