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FDA 510(k)

Profoject™ Pen Needles (Model A; Model B)

K 號:K260739 · 2026-07-15

決定日期2026-07-15
產品代碼FMI
諮詢委員會HO
決定Substantially Equivalent

器材摘要

Profoject™ Pen Needles (Model A; Model B) is the device name listed in this FDA 510(k) record. The listed applicant is CMT Health PTE., Ltd.. It received FDA 510(k) clearance on 2026-07-15 under 510(k) number K260739. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Profoject™ Pen Needles (Model A; Model B)?

Profoject™ Pen Needles (Model A; Model B) is a medical device that received FDA 510(k) clearance on 2026-07-15. The listed applicant is CMT Health PTE., Ltd.. The 510(k) number is K260739.

When did Profoject™ Pen Needles (Model A; Model B) receive FDA 510(k) clearance?

Profoject™ 鋼針筆(型號 A;型號 B)於2026-07-15獲得FDA 510(k)許可,許可編號K260739。

Who is the listed applicant for Profoject™ Pen Needles (Model A; Model B)?

The FDA 510(k) record lists CMT Health PTE., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Profoject™ Pen Needles (Model A; Model B)?

The FDA product code for Profoject™ Pen Needles (Model A; Model B) is FMI.

相關臨床試驗

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其他以 CMT Health PTE., Ltd. 為申請人之記錄

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相關器械(代碼:FMI)

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官方來源

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