腹腔镜避孕输卵管结扎装置
PMA编号：P870076 · 2021-05-19
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决定日期2021-05-19
PMA 编号P870076
产品代码KNH
设备分类第3类
医疗专科O
法规编号21 CFR 8
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
Laparoscopic contraceptive tubal occlusion device is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Acmi, Inc.. It received FDA 510(k) clearance on 2021-05-19. The device is classified under product code KNH. It was reviewed by the OB advisory panel.
常见问题
What is the Laparoscopic contraceptive tubal occlusion device?
Laparoscopic contraceptive tubal occlusion device is a medical device that received FDA 510(k) clearance on 2021-05-19. The listed applicant is Gyrus Acmi, Inc..
When did Laparoscopic contraceptive tubal occlusion device receive FDA 510(k) clearance?
The clearance date for Laparoscopic contraceptive tubal occlusion device can be found in the official FDA records.
Who is the listed applicant for Laparoscopic contraceptive tubal occlusion device?
The FDA 510(k) record lists Gyrus Acmi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Laparoscopic contraceptive tubal occlusion device?
The FDA product code for Laparoscopic contraceptive tubal occlusion device is KNH.
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官方来源
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