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FDA 510(k)

Profoject™ 一次性注射器,Profoject™ 一次性注射器带针

K号: K252033 · 2025-07-25

决定日期2025-07-25
产品代码FMF
咨询委员会HO
决定Substantially Equivalent

器械摘要

Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with 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 2025-07-25 under 510(k) number K252033. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with Needle?

Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with Needle is a medical device that received FDA 510(k) clearance on 2025-07-25. The listed applicant is CMT Health PTE., Ltd.. The 510(k) number is K252033.

When did Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with Needle receive FDA 510(k) clearance?

Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with Needle received FDA 510(k) clearance on 2025-07-25, under 510(k) number K252033.

Who is the listed applicant for Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with 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 Syringe, Profoject™ Disposable Syringe with Needle?

The FDA product code for Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with Needle is FMF.

相关临床试验

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列明CMT Health PTE., Ltd.为申报人的其他记录

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相关器械(代码:FMF)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。

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