Stimulator, electrical, implanted, for parkinsonian tremor
PMA 核准號：P140009 · 2026-09-23
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器材摘要
Stimulator, electrical, implanted, for parkinsonian tremor is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-09-23. The device is classified under product code MHY. It was reviewed by the NE advisory panel.
常見問題
What is the Stimulator, electrical, implanted, for parkinsonian tremor?
Stimulator, electrical, implanted, for parkinsonian tremor is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is ABBOTT MEDICAL.
When did Stimulator, electrical, implanted, for parkinsonian tremor receive FDA 510(k) clearance?
The clearance date for Stimulator, electrical, implanted, for parkinsonian tremor can be found in the official FDA records.
Who is the listed applicant for Stimulator, electrical, implanted, for parkinsonian tremor?
The FDA 510(k) record lists ABBOTT MEDICAL as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, electrical, implanted, for parkinsonian tremor?
The FDA product code for Stimulator, electrical, implanted, for parkinsonian tremor is MHY.
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