# Airlife, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 76 (1979–1984): 76 510(k) clearances
- Product codes: CAF (16), BZA (11), BYX (7), BYG (6), BYF (5), BZO (5), CAI (4), CBP (2), KFZ (2), BWF (2), KGB (2), BTT (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Impact Instrumentation, Inc.: 1 (https://510kreport.com/company/impact-instrumentation)
- Fisher & Paykel Healthcare, Ltd.: 1 (https://510kreport.com/company/fisher-paykel-healthcare)

## Its most-cited devices
- K801875: Circuits, Breathing W/Connectors, Adapt (1980), cited by 1
- K831246: Whistler in-Line Pressure Release Valve (1983), cited by 1

## Recent decisions
- K834570: Volume Ventilator Circuit W/Water Trap (Mar 5, 1984)
- K834573: Aqua Trap (Mar 5, 1984)
- K834077: Single Use Nebulizer-Adjust-Air Entrain (Dec 12, 1983)
- K833196: Volume Ventilator Circuit-Nebulizer (Nov 3, 1983)
- K833197: Trach Swive/Connector (Oct 28, 1983)
- K832725: Dual Dial Venturi Style Mask (Sep 20, 1983)
- K831246: Whistler in-Line Pressure Release Valve (Jul 26, 1983)
- K830895: Single Use Nebulizer, Adjust. Air- (Apr 28, 1983)

Source page: https://510kreport.com/company/airlife