TENS & EMS Stimulator (MHD-1083)— 510(k) K241678

Name: FDA 510(k) clearance K241678
Creator: U.S. Food and Drug Administration
Published: 2024-09-09

Substantially Equivalent

Shenzhen Minghuangda Electronics Co., Ltd.

FDA 510(k) clearance K241678 for TENS & EMS Stimulator (MHD-1083), Substantially Equivalent on 2024-09-09. Applicant: Shenzhen Minghuangda Electronics Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Minghuangda Electronics Co., Ltd.
Product code: Code NUH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2024-06-11
Decision date: 2024-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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K253896 — TENS/EMS device (GUSE01)2026-03-04
K253305 — TENS AND EMS (TENS and Muscle Stimulator) (JT1065, JT1080, JT2080, JT9034)2025-12-31
K251958 — VEINOPLUS Back2025-12-23

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