meddevicedb.com FDA Device Reference

BIPAP SYNCHRONY 2

K092043 Class II Special
Decision Date
2009-08-05
Sponsor / Applicant
Respironics, Inc.

Technical Specification

510(k) Submission ID K092043
Product Code MNS
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5895
Decision Date 2009-08-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIPAP SYNCHRONY 2 received FDA 510(k) clearance under submission number K092043, 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 2009-08-05.

Classification & Regulation

This clearance is catalogued under FDA product code MNS and 21 CFR 868.5895, within the Anesthesiology review panel as a Class II device.