FDA cleared the Wearable ECG Recorder (YMHeart XY-12); Wearable ECG Recorder (YMHeart XY-1201); Wearable ECG Recorder (YMHeart XY-1202); Wearable ECG Recorder (YMHeart XY-1203); Wearable ECG Recorder (YMHeart XY-03); Wearable ECG Recorder (YMHeart XY-0301); Wearable ECG Recorder (YMHeart XY-0302); Wearable ECG Recorder (YMHeart XY-0303) from Shenzhen Xinyan Medical Technology Co.,ltd. on Sep 11, 2026 under K254119, a traditional 510(k). The device falls under product code MWJ, Electrocardiograph, Ambulatory (Without Analysis), regulated at 21 CFR 870.2800 as a Class 2 device. The review panel was Cardiovascular.
FDA logged the submission as received on Dec 19, 2025. The decision came 266 days later, longer than the 90 FDA-day review goal, which usually means at least one additional information request.
This is the only decision on file for Shenzhen Xinyan Medical Technology Co.,ltd. in the last 12 months of the tracker.
Questions & Answers
What did FDA clear under K254119?
K254119 is the FDA 510(k) for Wearable ECG Recorder (YMHeart XY-12); Wearable ECG Recorder (YMHeart XY-1201); Wearable ECG Recorder (YMHeart XY-1202); Wearable ECG Recorder (YMHeart XY-1203); Wearable ECG Recorder (YMHeart XY-03); Wearable ECG Recorder (YMHeart XY-0301); Wearable ECG Recorder (YMHeart XY-0302); Wearable ECG Recorder (YMHeart XY-0303), submitted by Shenzhen Xinyan Medical Technology Co.,ltd.. FDA's decision date was Sep 11, 2026, under product code MWJ (Electrocardiograph, Ambulatory (Without Analysis)).
Who makes the Wearable ECG Recorder (YMHeart XY-12); Wearable ECG Recorder (YMHeart XY-1201); Wearable ECG Recorder (YMHeart XY-1202); Wearable ECG Recorder (YMHeart XY-1203); Wearable ECG Recorder (YMHeart XY-03); Wearable ECG Recorder (YMHeart XY-0301); Wearable ECG Recorder (YMHeart XY-0302); Wearable ECG Recorder (YMHeart XY-0303)?
Shenzhen Xinyan Medical Technology Co.,ltd., based in Shenzhen, is the applicant of record for K254119.
How long did the K254119 review take?
FDA received the submission on Dec 19, 2025 and issued its decision on Sep 11, 2026, 266 days later.