K-number	K031081
Device name	EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS
Applicant	Gyrus Medical, Inc.
Product code	GEI
Device class	Class II
Decision date	May 21, 2003
Decision	Substantially Equivalent
Regulation	—

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 →

EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS

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