K-number	K050843
Device name	AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM
Applicant	Xoft, Inc.
Product code	JAD
Device class	Class II
Decision date	Dec 22, 2005
Decision	Unknown
Regulation	892.5900

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 →

AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM

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