FDA PMA

设备，热消融，子宫内膜

PMA编号：P000032 · 2018-07-11

申请人CooperSurgical, Inc.

决定日期2018-07-11

PMA 编号P000032

产品代码MNB

设备分类第3类

医疗专科U

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。

器械摘要

Device, thermal ablation, endometrial is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 2018-07-11. The device is classified under product code MNB. It was reviewed by the OB advisory panel.

常见问题

What is the Device, thermal ablation, endometrial?

Device, thermal ablation, endometrial is a medical device that received FDA 510(k) clearance on 2018-07-11. The listed applicant is CooperSurgical, Inc..

When did Device, thermal ablation, endometrial receive FDA 510(k) clearance?

The clearance date for Device, thermal ablation, endometrial can be found in the official FDA records.

设备、热消融、子宫内膜的列名申请人是谁？

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。

什么是设备、热消融、子宫内膜的FDA产品代码？

FDA产品代码为设备、热消融、子宫内膜的是MNB。

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。

器械摘要

常见问题

相关临床试验

官方来源