K-number	K092797
Device name	ACUTE AND CHRONIC CATHETER REPAIR KIT
Applicant	Kendall
Product code	NFK
Device class	Class II
Decision date	Nov 19, 2009
Decision	Unknown
Regulation	876.5540

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 →

ACUTE AND CHRONIC CATHETER REPAIR KIT

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