K-number	K801289
Device name	LEECO GLYCO-HEMOGLOBIN DIAG. TEST KIT
Applicant	Leeco Diagnostics, Inc.
Product code	LCP
Device class	Class II
Decision date	Jun 30, 1980
Decision	Substantially Equivalent
Regulation	864.7470

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 →

LEECO GLYCO-HEMOGLOBIN DIAG. TEST KIT

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