电植入式刺激器，用于帕金森症状
PMA编号：P150031 · 2026-09-22
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决定日期2026-09-22
PMA 编号P150031
产品代码NHL
设备分类第3类
医疗专科U
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
器械摘要
Stimulator, electrical, implanted, for parkinsonian symptoms 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 2026-09-22. The device is classified under product code NHL. It was reviewed by the NE advisory panel.
常见问题
What is the Stimulator, electrical, implanted, for parkinsonian symptoms?
Stimulator, electrical, implanted, for parkinsonian symptoms is a medical device that received FDA 510(k) clearance on 2026-09-22. The listed applicant is Boston Scientific Corp.
When did Stimulator, electrical, implanted, for parkinsonian symptoms receive FDA 510(k) clearance?
The clearance date for Stimulator, electrical, implanted, for parkinsonian symptoms can be found in the official FDA records.
谁是用于帕金森症状的植入式电刺激器的列名申请人？
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
什么是用于帕金森症状的植入式电刺激器的FDA产品代码？
FDA产品代码为用于帕金森症状的植入式电刺激器的代码是NHL。
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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