Airlife, Inc. - FDA 510(k) Cleared Devices
76
Total
76
Cleared
0
Denied
FDA 510(k) Regulatory Record - Airlife, Inc. Anesthesiology ✕
71 devices
Cleared
Mar 05, 1984
VOLUME VENTILATOR CIRCUIT W/WATER TRAP
Anesthesiology
67d
Cleared
Mar 05, 1984
AQUA TRAP
Anesthesiology
67d
Cleared
Dec 12, 1983
SINGLE USE NEBULIZER-ADJUST-AIR ENTRAIN
Anesthesiology
17d
Cleared
Nov 03, 1983
VOLUME VENTILATOR CIRCUIT-NEBULIZER
Anesthesiology
45d
Cleared
Oct 28, 1983
TRACH SWIVE/CONNECTOR
Anesthesiology
39d
Cleared
Sep 20, 1983
DUAL DIAL VENTURI STYLE MASK
Anesthesiology
39d
Cleared
Jul 26, 1983
WHISTLER IN-LINE PRESSURE RELEASE VALVE
Anesthesiology
99d
Cleared
Apr 28, 1983
SINGLE USE NEBULIZER, ADJUST. AIR-
Anesthesiology
38d
Cleared
Apr 18, 1983
HUMIDIFIER, WITH OR WITHOUT ADAPTER
Anesthesiology
28d
Cleared
May 18, 1982
AIRLIFE NEBULIZER HEATER
Anesthesiology
28d
Cleared
May 13, 1982
DISPOSABLE THERMOPLASTIC RUBBER MOUTH
Anesthesiology
23d
Cleared
Aug 12, 1981
INSPIRATORY FORCE PRESSURE ADAPTOR
Anesthesiology
22d
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