FDA 510(k)

S21 OTC Transcutaneous Electrical Nerve Stimulator

Número K: K233095 · 2024-03-01

RequerenteMicro Current Technology, Inc.

Data da decisão2024-03-01

Código do produtoNUH

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

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