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RESPIRONICS SLEEPEASY CPAP SYSTEM

K091112 Class II Special
Decision Date
2009-05-15
Sponsor / Applicant
Respironics, Inc.

Technical Specification

510(k) Submission ID K091112
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2009-05-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESPIRONICS SLEEPEASY CPAP SYSTEM received FDA 510(k) clearance under submission number K091112, sponsored by Respironics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2009-05-15.

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.