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EASYCARE TX SYSTEM (CONNEXUNS)

K113780 Class II Traditional
Decision Date
2012-04-20
Sponsor / Applicant
Resmed, Ltd.

Technical Specification

510(k) Submission ID K113780
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2012-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYCARE TX SYSTEM (CONNEXUNS) received FDA 510(k) clearance under submission number K113780, sponsored by Resmed, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2012-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.