K-number	K953511
Device name	KENDALL SHERIDAN CPAP SYSTEM
Applicant	Kendall Healthcare Products Co. Div.Of Tyco Health
Product code	BYE
Device class	Class II
Decision date	Oct 26, 1995
Decision	Unknown
Regulation	868.5965

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 →

KENDALL SHERIDAN CPAP SYSTEM

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