FDA 510(k), K151901, AirView

510(K) Number: K151901
Device Name: AirView
Manufacturer: RESMED LTD.
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 07/10/2015
Decision Date: 11/05/2015
Regulation Medical Specialty: Anesthesiology

209 pages (2,284 of 2,493 original pages are fully redacted)