Back to free search
Home / Search / K781751

CATHETER, AKRON FOLEY TEFLON

Latex Ind., Inc. · Class II · Cleared Jan 22, 1979

K-numberK781751
Device nameCATHETER, AKRON FOLEY TEFLON
ApplicantLatex Ind., Inc.
Product codeKOD
Device classClass II
Decision dateJan 22, 1979
DecisionSubstantially Equivalent
Regulation876.5130
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 →

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

14-day free trial. No setup. Cancel anytime.

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 →