FDA PMA

Stimulator, carotid sinus nerve

PMA Number: P180050 · 2025-07-11

ApplicantCvrx, Inc.

Decision Date2025-07-11

PMA NumberP180050

Product CodeDSR

Device ClassClass 3

Medical SpecialtyC

Regulation Number21 CFR 8

Advisory CommitteeCV

Device Summary

Stimulator, carotid sinus nerve is the device name listed in this FDA 510(k) record. The listed applicant is Cvrx, Inc.. It received FDA 510(k) clearance on 2025-07-11. The device is classified under product code DSR. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Stimulator, carotid sinus nerve?

Stimulator, carotid sinus nerve is a medical device that received FDA 510(k) clearance on 2025-07-11. The listed applicant is Cvrx, Inc..

When did Stimulator, carotid sinus nerve receive FDA 510(k) clearance?

The clearance date for Stimulator, carotid sinus nerve can be found in the official FDA records.

Who is the listed applicant for Stimulator, carotid sinus nerve?

The FDA 510(k) record lists Cvrx, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stimulator, carotid sinus nerve?

The FDA product code for Stimulator, carotid sinus nerve is DSR.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.