K-number	K101242
Device name	GENESIS DM MODEL: 6053000A1
Applicant	Honeywell Hommed, LLC
Product code	DRG
Device class	Class II
Decision date	Jun 11, 2010
Decision	Substantially Equivalent
Regulation	870.2910

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 →

GENESIS DM MODEL: 6053000A1

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