FDA 510(k)

真空泵（型号：AD-VPUM-500）

K号: K260194 · 2026-04-28

申请人Sheng Sheng Yi (Beijing) Technology Company Limited

决定日期2026-04-28

产品代码MQG

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决定实质等同

器械摘要

Vacuum Pump (Model: AD-VPUM-500) is the device name listed in this FDA 510(k) record. The listed applicant is Sheng Sheng Yi (Beijing) Technology Company Limited. It received FDA 510(k) clearance on 2026-04-28 under 510(k) number K260194. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Vacuum Pump (Model: AD-VPUM-500)?

Vacuum Pump (Model: AD-VPUM-500) is a medical device that received FDA 510(k) clearance on 2026-04-28. The listed applicant is Sheng Sheng Yi (Beijing) Technology Company Limited. The 510(k) number is K260194.

When did Vacuum Pump (Model: AD-VPUM-500) receive FDA 510(k) clearance?

Vacuum Pump (Model: AD-VPUM-500) received FDA 510(k) clearance on 2026-04-28, under 510(k) number K260194.

Who is the listed applicant for Vacuum Pump (Model: AD-VPUM-500)?

The FDA 510(k) record lists Sheng Sheng Yi (Beijing) Technology Company Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vacuum Pump (Model: AD-VPUM-500)?

The FDA product code for Vacuum Pump (Model: AD-VPUM-500) is MQG.

相关器械（代码：MQG）

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。

K261083华莱士® 吸引泵（WAPV1）；华莱士® 泵过滤器连接器（WFC）；华莱士® 真空连接套件（WVCK）CooperSurgical, Inc.K242684Harioculture TL-16 Time-lapse IncubatorHua Yue Medical Technology Co., Ltd.K232493Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004)Wuhan Huchuang Union Technology Co., Ltd.K180188Geri 胚胎孵化器，配备 Geri Connect 和 Geri 评估软件，以及 Geri 碗Genea Biomedx Pty, Ltd.K173264EmbryoScope+Vitrolife A/S K180304Geri 胚胎孵化器和 Geri 碗Genea Biomedx Pty, Ltd.

官方来源

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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。

器械摘要

常见问题

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相关器械（代码：MQG）

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