AD-2126 Transcutaneous Electrical Nerve Stimulators (TENS)

FDA 510(k) K222867 · Andon Health Co, Ltd.

Substantially Equivalent

510(k) numberK222867

Submission

Device name
AD-2126 Transcutaneous Electrical Nerve Stimulators (TENS)
Applicant
Andon Health Co, Ltd.
Tianjin, CN
Received
September 22, 2022
Decision date
December 21, 2022
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NUH – Stimulator, Nerve, Transcutaneous, Over-The-Counter
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5890
Specialty
Neurology

TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES

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Questions and answers

When was AD-2126 Transcutaneous Electrical Nerve Stimulators (TENS) cleared by the FDA?

AD-2126 Transcutaneous Electrical Nerve Stimulators (TENS) (K222867) received a 510(k) decision of Substantially Equivalent on December 21, 2022, 90 days after the submission was received.

What is the product code of K222867?

The FDA product code is NUH – Stimulator, Nerve, Transcutaneous, Over-The-Counter, a Class II (moderate risk) device regulated under 21 CFR 882.5890.