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FDA 510(k)

Transcutaneous Electrical Nerve Stimulator (9029SCM)

K-Number: K240292 · 2024-03-25

Decision Date2024-03-25
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Transcutaneous Electrical Nerve Stimulator (9029SCM) is a medical device manufactured by Hong Kong Etech Groups Limited. It received FDA 510(k) clearance on 2024-03-25 under approval number K240292. 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 Transcutaneous Electrical Nerve Stimulator (9029SCM)?

Transcutaneous Electrical Nerve Stimulator (9029SCM) is a medical device that received FDA 510(k) clearance on 2024-03-25. It is manufactured by Hong Kong Etech Groups Limited. The 510(k) number is K240292.

When was Transcutaneous Electrical Nerve Stimulator (9029SCM) approved by the FDA?

Transcutaneous Electrical Nerve Stimulator (9029SCM) received FDA 510(k) clearance on 2024-03-25, under approval number K240292.

What company makes Transcutaneous Electrical Nerve Stimulator (9029SCM)?

Transcutaneous Electrical Nerve Stimulator (9029SCM) is manufactured by Hong Kong Etech Groups Limited.

What is the FDA product code for Transcutaneous Electrical Nerve Stimulator (9029SCM)?

The FDA product code for Transcutaneous Electrical Nerve Stimulator (9029SCM) is NUH.

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Official Source

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