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Huinno Co., Ltd.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest FDA decision2025-12-05
TypeNumberDevice NameCodeDateActions
510(k) K243438 MEMO Patch M (MPT-E08R-UNC01)DXH2025-12-05 View

Related Clinical Trials

NCT07722026This Exploratory Medical Device Study Evaluated the Arrhythmia Diagnostic Yield of MEMO Patch V2, a Wearable Patch-type Electrocardiographic Monitor, in Adults With Suspected Arrhythmia Who Presented With Symptoms Such as Palpitations or Dizziness, or Who Had Cryptogenic Ischemic Stroke or TransientCOMPLETEDNCT07722039Clinical Validation of SMD-RVECG for Predicting Atrial Fibrillation With Rapid Ventricular Response Within 2 HoursNOT_YET_RECRUITINGNCT07725445Evaluation of an AI-Based Lightweight ECG Telemetry Monitoring SystemCOMPLETEDNCT077285527-Day MEMO Patch Monitoring for Arrhythmia Detection in Patients With PalpitationsCOMPLETEDNCT07736066Remote ECG Monitoring-Based Phase I Cardiac Rehabilitation After Heart SurgeryCOMPLETEDNCT07792772Arrhythmia Detection With MEMO Patch Plus in Patients With Acute Heart FailureCOMPLETED
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