Stimulator, electrical, implanted, for parkinsonian symptoms
PMA 번호: P150031 · 2026-09-22
광고
기기 요약
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.
자주 묻는 질문
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.
관련 임상시험
관련 기록은 이름, 제품 코드 또는 기타 메타데이터를 사용하여 자동으로 매칭됩니다. 매칭은 검증된 임상, 과학, 기업 또는 규제 상의 관계를 입증하지 않으며, 연결된 공식 출처를 검토하시기 바랍니다.
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공식 출처
FDA 데이터베이스에서 보기 →FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.
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