Stimulator, electrical, implanted, for parkinsonian symptoms
PMA Number: P150031 · 2026-09-22
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Device Summary
Frequently Asked Questions
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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