Stimulator, electrical, implanted, for parkinsonian symptoms
PMA番号：P150031 · 2026-09-22
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医療機器の概要
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.
よくある質問
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.
Who is the listed applicant for Stimulator, electrical, implanted, for parkinsonian symptoms?
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 Stimulator, electrical, implanted, for parkinsonian symptoms?
The FDA product code for Stimulator, electrical, implanted, for parkinsonian symptoms is NHL.
関連する臨床試験
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公式ソース
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