FDA 510(k)

ALLY II子宫定位系统™（UPS）

K号: K223064 · 2022-10-28

决定日期2022-10-28

产品代码LKF

咨询委员会OB 请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。

决定实质等同

器械摘要

ALLY II Uterine Positioning System™ (UPS) is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 2022-10-28 under 510(k) number K223064. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ALLY II Uterine Positioning System™ (UPS)?

ALLY II Uterine Positioning System™ (UPS) is a medical device that received FDA 510(k) clearance on 2022-10-28. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K223064.

When did ALLY II Uterine Positioning System™ (UPS) receive FDA 510(k) clearance?

ALLY II Uterine Positioning System™ (UPS) received FDA 510(k) clearance on 2022-10-28, under 510(k) number K223064.

Who is the listed applicant for ALLY II Uterine Positioning System™ (UPS)?

FDA 510(k)记录中列出CooperSurgical, Inc.为申请人。这本身并不足以确立设备制造商。

What is the FDA product code for ALLY II Uterine Positioning System™ (UPS)?

The FDA product code for ALLY II Uterine Positioning System™ (UPS) is LKF.

列明CooperSurgical, Inc.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。

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）K243799复杂腹裂胎儿修复：一项安全性和可行性试验 K250438CooperSurgical Milex® 子宫托 K201086Advincula Delineator 宫腔操纵器 K200038Endosee System K191020G210 InviCell Plus with SignipHy pH 监测

查看所有 16 个设备 →

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。