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FDA 510(k)

S21 OTC Transcutaneous Electrical Nerve Stimulator

K-Number: K233095 · 2024-03-01

ApplicantMicro Current Technology, Inc.
Decision Date2024-03-01
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

S21 OTC Transcutaneous Electrical Nerve Stimulator is a medical device manufactured by Micro Current Technology, Inc.. It received FDA 510(k) clearance on 2024-03-01 under approval number K233095. 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 S21 OTC Transcutaneous Electrical Nerve Stimulator?

S21 OTC Transcutaneous Electrical Nerve Stimulator is a medical device that received FDA 510(k) clearance on 2024-03-01. It is manufactured by Micro Current Technology, Inc.. The 510(k) number is K233095.

When was S21 OTC Transcutaneous Electrical Nerve Stimulator approved by the FDA?

S21 OTC Transcutaneous Electrical Nerve Stimulator received FDA 510(k) clearance on 2024-03-01, under approval number K233095.

What company makes S21 OTC Transcutaneous Electrical Nerve Stimulator?

S21 OTC Transcutaneous Electrical Nerve Stimulator is manufactured by Micro Current Technology, Inc..

What is the FDA product code for S21 OTC Transcutaneous Electrical Nerve Stimulator?

The FDA product code for S21 OTC Transcutaneous Electrical Nerve Stimulator is NUH.

Related Clinical Trials

NCT07517172 Evaluating Noninvasive Brain Stimulation for TMD Pain: A Feasibility Study RECRUITING NCT03053791 Deep Brain Stimulation in Patients With Incomplete Spinal Cord Injury for Improvement of Gait RECRUITING NCT06816004 Noninvasive Vagal Nerve Stimulation ACTIVE_NOT_RECRUITING NCT07614945 Effect of Reflexology on Pain and Sleep Disorders in Females With Fibromyalgia NOT_YET_RECRUITING NCT06127550 taVNS for Letter Learning in Dyslexia SUSPENDED NCT07610655 Effects of Transcutaneous Vagal Nerve Stimulation on Post-Surgical Return to Consciousness, Delirium, and Depression RECRUITING

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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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