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FDA 510(k)

Nu-beca Transcutaneous Electrical Nerve Stimulation

K-Number: K223151 · 2023-07-19

ApplicantNu-Beca & Maxcellent Co.
Decision Date2023-07-19
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Nu-beca Transcutaneous Electrical Nerve Stimulation is a medical device manufactured by Nu-Beca & Maxcellent Co.. It received FDA 510(k) clearance on 2023-07-19 under approval number K223151. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nu-beca Transcutaneous Electrical Nerve Stimulation?

Nu-beca Transcutaneous Electrical Nerve Stimulation is a medical device that received FDA 510(k) clearance on 2023-07-19. It is manufactured by Nu-Beca & Maxcellent Co.. The 510(k) number is K223151.

When was Nu-beca Transcutaneous Electrical Nerve Stimulation approved by the FDA?

Nu-beca Transcutaneous Electrical Nerve Stimulation received FDA 510(k) clearance on 2023-07-19, under approval number K223151.

What company makes Nu-beca Transcutaneous Electrical Nerve Stimulation?

Nu-beca Transcutaneous Electrical Nerve Stimulation is manufactured by Nu-Beca & Maxcellent Co..

What is the FDA product code for Nu-beca Transcutaneous Electrical Nerve Stimulation?

The FDA product code for Nu-beca Transcutaneous Electrical Nerve Stimulation is NUH.

Related Clinical Trials

NCT05452226 Neuromuscular Electrical Stimulation in COPD/Community Acquired Pneumonia COMPLETED NCT06998134 Toward Ubiquitous Lower Limb Exoskeleton Use in Children and Young Adults RECRUITING NCT06868914 Phase I Trial of High-Density Theta Burst Stimulation (hdTBS) NOT_YET_RECRUITING NCT04935697 Non-invasive Vagal Neurostimulation (nVNS) for Traumatic Brain Injury (TBI)-Induced Acute Respiratory Distress COMPLETED NCT01961557 Evaluating a New Knee-Ankle-Foot Brace to Improve Gait in Children With Movement Disorders COMPLETED NCT06577454 Measuring the Effects of Neurostimulation on Risky and Ambiguous Decision-Making Capacity in People With and Without Substance Use Disorder SUSPENDED

Related PubMed Literature

PMID: 41470022 Low-intensity pulsed ultrasound for peripheral nerve regeneration: mechanobiological mechanisms and translational potential. Journal of translational medicine (2025)

Related Devices (Code: NUH)

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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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