K-number	K193602
Device name	LV Liberty Vision Model 1 90Yttrium Brachytherapy Source
Applicant	Lv Liberty Vision Corporation
Product code	KXK
Device class	Class II
Decision date	May 29, 2020
Decision	Substantially Equivalent
Regulation	892.5730

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 →

LV Liberty Vision Model 1 90Yttrium Brachytherapy Source

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