FDA 510(k)

Profoject™ LOR Syringe

K号: K261372 · 2026-09-25

决定日期2026-09-25

产品代码CAZ

咨询委员会AN

决定Substantially Equivalent

器械摘要

Profoject™ LOR Syringe 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 2026-09-25 under 510(k) number K261372. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Profoject™ LOR Syringe?

Profoject™ LOR Syringe is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is CMT Health PTE., Ltd.. The 510(k) number is K261372.

When did Profoject™ LOR Syringe receive FDA 510(k) clearance?

Profoject™ LOR Syringe received FDA 510(k) clearance on 2026-09-25, under 510(k) number K261372.

Who is the listed applicant for Profoject™ LOR Syringe?

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™ LOR Syringe?

The FDA product code for Profoject™ LOR Syringe is CAZ.

列明CMT Health PTE., Ltd.为申报人的其他记录

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。

K262215Profoject™ Safety Sliding Blood Collection Set K261829Profoject™ Dual-Safety Pen Needles K260739Profoject™ Pen Needles (Model A; Model B)K260514Profoject™ 安全针；Profoject™ 带安全针的注射器；Profoject™ 低死腔注射器带安全针 K260855Profoject™ 安全笔针 K253268Profoject 鼻饲/口饲注射器；Profoject 可重复使用鼻饲/口饲注射器（型号A，型号B）；Profoject ENFit 连接器；Profoject 鼻饲注射器盖

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