FDA 510(k)Profoject™ Disposable Needle
K 號:K252631 · 2025-10-16
決定日期2025-10-16
產品代碼FMI
諮詢委員會HO
決定Substantially Equivalent
器材摘要
Profoject™ Disposable Needle 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 2025-10-16 under 510(k) number K252631. 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™ Disposable Needle?
Profoject™ Disposable Needle is a medical device that received FDA 510(k) clearance on 2025-10-16. The listed applicant is CMT Health PTE., Ltd.. The 510(k) number is K252631.
When did Profoject™ Disposable Needle receive FDA 510(k) clearance?
Profoject™ Disposable Needle received FDA 510(k) clearance on 2025-10-16, under 510(k) number K252631.
Who is the listed applicant for Profoject™ Disposable Needle?
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™ Disposable Needle?
The FDA product code for Profoject™ Disposable Needle is FMI.
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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)
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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