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FDA PMA

Stimulator, electrical, implanted, for parkinsonian tremor

PMA Number: P140009 · 2026-09-23

ApplicantABBOTT MEDICAL
Decision Date2026-09-23
PMA NumberP140009
Product CodeMHY
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeNE

Device Summary

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.

Frequently Asked Questions

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.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

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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