Medical Device Manufacturer · US , Mchenry , IL

Airlife, Inc. - FDA 510(k) Cleared Devices

76 submissions · 76 cleared · Since 1979

Total

Cleared

Denied

Airlife, Inc. has 76 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 76 cleared submissions from 1979 to 1984.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Airlife, Inc.

76 devices

1-12 of 76

Cleared Mar 05, 1984

VOLUME VENTILATOR CIRCUIT W/WATER TRAP

SINGLE USE NEBULIZER-ADJUST-AIR ENTRAIN

K834077 · CAF

Anesthesiology · 17d

Cleared Nov 03, 1983

VOLUME VENTILATOR CIRCUIT-NEBULIZER

K833196 · CAI

Anesthesiology · 45d

Cleared Oct 28, 1983

TRACH SWIVE/CONNECTOR

K833197 · BTR

Anesthesiology · 39d

Cleared Sep 20, 1983

DUAL DIAL VENTURI STYLE MASK

K832725 · BYF

Anesthesiology · 39d

Cleared Jul 26, 1983

WHISTLER IN-LINE PRESSURE RELEASE VALVE

K831246 · CBP

Anesthesiology · 99d

Cleared Apr 28, 1983

SINGLE USE NEBULIZER, ADJUST. AIR-

K830895 · CAF

Anesthesiology · 38d

Cleared Apr 18, 1983

HUMIDIFIER, WITH OR WITHOUT ADAPTER

K830896 · KFZ

Anesthesiology · 28d

Cleared May 18, 1982

AIRLIFE NEBULIZER HEATER

K821129 · CAF

Anesthesiology · 28d

Cleared May 13, 1982

DISPOSABLE THERMOPLASTIC RUBBER MOUTH

K821128 · BYP

Anesthesiology · 23d

Cleared Aug 12, 1981

INSPIRATORY FORCE PRESSURE ADAPTOR

K812067 · BZA

Anesthesiology · 22d

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Airlife, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Airlife, Inc.

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