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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 the device name listed in this FDA 510(k) record. The listed applicant is Micro Current Technology, Inc.. It received FDA 510(k) clearance on 2024-03-01 under 510(k) 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. The listed applicant is Micro Current Technology, Inc.. The 510(k) number is K233095.

When did S21 OTC Transcutaneous Electrical Nerve Stimulator receive FDA 510(k) clearance?

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

Who is the listed applicant for S21 OTC Transcutaneous Electrical Nerve Stimulator?

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

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

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Other records listing Micro Current Technology, Inc. as applicant

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.

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Related Devices (Code: NUH)

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.

K260412TENS 7000 Rechargeable 4 Channel (TENS 7000H)Shenzhen Dongdixin Technology Co., Ltd.K260425TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)Hivox Biotek, Inc.K253896TENS/EMS device (GUSE01)Globalcare Medical Technology Co., Ltd.K253305TENS AND EMS (TENS and Muscle Stimulator) (JT1065, JT1080, JT2080, JT9034)Shenzhen Jiantuo Electronics Co., Ltd.K253740TENS&EMS (HZ9151B, HZ9151C, HZ9151D)Hong Qiangxing (Shenzhen) Electronics LimitedK251958VEINOPLUS BackDynapulse Medical

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.

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