FDA 510(k)

MOLLI 2 系统

K号: K253888 · 2025-12-31

决定日期2025-12-31

产品代码NEU

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决定实质等同

器械摘要

MOLLI 2 System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2025-12-31 under 510(k) number K253888. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MOLLI 2 System?

MOLLI 2 System is a medical device that received FDA 510(k) clearance on 2025-12-31. The listed applicant is Stryker Endoscopy. The 510(k) number is K253888.

When did MOLLI 2 System receive FDA 510(k) clearance?

MOLLI 2 System received FDA 510(k) clearance on 2025-12-31, under 510(k) number K253888.

Who is the listed applicant for MOLLI 2 System?

FDA 510(k)记录显示Stryker Endoscopy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 MOLLI 2 System?

The FDA product code for MOLLI 2 System is NEU.

列明Stryker Endoscopy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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相关器械（代码：NEU）

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。

K253761HydroMARK™ Plus 乳腺活检位点标记（蜻蜓形状）；HydroMARK™ Plus 乳腺活检位点标记（蜂鸟形状）Devicor Medical Products, Inc.K252892SCOUT MD 外科引导系统Merit Medical Systems, Inc.K251989VizMark 预装组织标记器设备（VM-0001）Breast-Med, Inc.K251748MammoSTAR活检位点标识器Carbon Medical Technologies, Inc.K243642UltraCor™ Twirl™ 乳腺组织标记器Bard Peripheral Vascular, Inc.K233639SmartClip 安全软组织标记Elucent Medical, Inc.

官方来源

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