植入式粪便失禁装置
PMA编号：P010020 · 2016-02-04
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决定日期2016-02-04
PMA 编号P010020
产品代码MIP
设备分类第3类
医疗专科U
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
器械摘要
Implanted fecal incontinence device is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2016-02-04. The device is classified under product code MIP. It was reviewed by the GU advisory panel.
常见问题
What is the Implanted fecal incontinence device?
Implanted fecal incontinence device is a medical device that received FDA 510(k) clearance on 2016-02-04. The listed applicant is Boston Scientific Corp.
When did Implanted fecal incontinence device receive FDA 510(k) clearance?
The clearance date for Implanted fecal incontinence device can be found in the official FDA records.
Who is the listed applicant for Implanted fecal incontinence device?
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Implanted fecal incontinence device?
The FDA product code for Implanted fecal incontinence device is MIP.
相关临床试验
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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。
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