刺激器，自主神经，植入用于中风康复
PMA编号：P210007 · 2026-09-16
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决定日期2026-09-16
PMA 编号P210007
产品代码QPY
设备分类第3类
医疗专科U
咨询委员会PM
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
Stimulator, autonomic nerve, implanted for stroke rehabilitation is the device name listed in this FDA 510(k) record. The listed applicant is Mobia Medical, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code QPY. It was reviewed by the PM advisory panel.
常见问题
What is the Stimulator, autonomic nerve, implanted for stroke rehabilitation?
Stimulator, autonomic nerve, implanted for stroke rehabilitation is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Mobia Medical, Inc..
When did Stimulator, autonomic nerve, implanted for stroke rehabilitation receive FDA 510(k) clearance?
The clearance date for Stimulator, autonomic nerve, implanted for stroke rehabilitation can be found in the official FDA records.
谁是植入式自主神经刺激器用于中风康复的列名申请人？
The FDA 510(k) record lists Mobia Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA产品代码是什么，用于植入式自主神经刺激器，用于中风康复？
FDA产品代码为用于中风康复的植入式自主神经刺激器为QPY。
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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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