FDA 510(k)

Luer-Split MAJ-2092

K号: K241842 · 2025-03-19

决定日期2025-03-19

产品代码ODC

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决定实质等同

器械摘要

Luer-Split MAJ-2092 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2025-03-19 under 510(k) number K241842. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Luer-Split MAJ-2092?

Luer-Split MAJ-2092 is a medical device that received FDA 510(k) clearance on 2025-03-19. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K241842.

When did Luer-Split MAJ-2092 receive FDA 510(k) clearance?

Luer-Split MAJ-2092 received FDA 510(k) clearance on 2025-03-19, under 510(k) number K241842.

Who is the listed applicant for Luer-Split MAJ-2092?

FDA 510(k)记录显示，Olympus Medical Systems Corporation为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Luer-Split MAJ-2092?

The FDA product code for Luer-Split MAJ-2092 is ODC.

列明Olympus Medical Systems Corporation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。

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