Counter OTC TENS Device, Model CSD-737Z

FDA 510(k) K151279 · Counter Scientific Development (Gz), Ltd.

Substantially Equivalent

510(k) numberK151279

Submission

Device name
Counter OTC TENS Device, Model CSD-737Z
Applicant
Counter Scientific Development (Gz), Ltd.
Guangzhou, CN
Received
May 14, 2015
Decision date
December 16, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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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More from Sigma Biomedical

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K161537OTC TENS Device, Model PTS-IVNUH · Traditional 10/13/2016SE
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Questions and answers

When was Counter OTC TENS Device, Model CSD-737Z cleared by the FDA?

Counter OTC TENS Device, Model CSD-737Z (K151279) received a 510(k) decision of Substantially Equivalent on December 16, 2015, 216 days after the submission was received.

What is the product code of K151279?

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