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FDA 510(k)

TENS & EMS Stimulator (MHD-1083)

K-Number: K241678 · 2024-09-09

ApplicantShenzhen Minghuangda Electronics Co., Ltd.
Decision Date2024-09-09
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS & EMS Stimulator (MHD-1083) is a medical device manufactured by Shenzhen Minghuangda Electronics Co., Ltd.. It received FDA 510(k) clearance on 2024-09-09 under approval number K241678. 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 TENS & EMS Stimulator (MHD-1083)?

TENS & EMS Stimulator (MHD-1083) is a medical device that received FDA 510(k) clearance on 2024-09-09. It is manufactured by Shenzhen Minghuangda Electronics Co., Ltd.. The 510(k) number is K241678.

When was TENS & EMS Stimulator (MHD-1083) approved by the FDA?

TENS & EMS Stimulator (MHD-1083) received FDA 510(k) clearance on 2024-09-09, under approval number K241678.

What company makes TENS & EMS Stimulator (MHD-1083)?

TENS & EMS Stimulator (MHD-1083) is manufactured by Shenzhen Minghuangda Electronics Co., Ltd..

What is the FDA product code for TENS & EMS Stimulator (MHD-1083)?

The FDA product code for TENS & EMS Stimulator (MHD-1083) is NUH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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