设备，热消融，子宫内膜
PMA编号：P970021 · 2016-01-04
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器械摘要
Device, thermal ablation, endometrial is the device name listed in this FDA 510(k) record. The listed applicant is Gynecare, Inc.. It received FDA 510(k) clearance on 2016-01-04. 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 2016-01-04. The listed applicant is Gynecare, 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.
Who is the listed applicant for Device, thermal ablation, endometrial?
The FDA 510(k) record lists Gynecare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Device, thermal ablation, endometrial?
The FDA product code for Device, thermal ablation, endometrial is MNB.
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官方来源
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