K-number	K030221
Device name	MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR
Applicant	Mytech Technology Co., Ltd.
Product code	DXN
Device class	Class II
Decision date	Jul 25, 2003
Decision	Substantially Equivalent
Regulation	870.1130

AI Summary

AI extraction for this record is queued and will appear within 24 hours. View full FDA record →

Source

View the full FDA submission: accessdata.fda.gov

Researching this as a predicate?

Want a transparent AI-ranking score, AI-discovered related predicates, ongoing safety and warning-letter monitoring, full predicate chain lineage, and a drafted SE rationale — all saved to your own project? That's what an account adds.

Start free trial →

Building an AI or ML-enabled device? Predicate search, PCCP tracking, and AI-specific FDA intelligence — built exclusively for AI/ML devices. Try AIFDA Intel →

MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR

Everything you need for a 510(k) submission. Nothing you don't.