Airlife, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
76
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K834570VOLUME VENTILATOR CIRCUIT W/WATER TRAPMarch 5, 1984
K834573AQUA TRAPMarch 5, 1984
K834077SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINDecember 12, 1983
K833196VOLUME VENTILATOR CIRCUIT-NEBULIZERNovember 3, 1983
K833197TRACH SWIVE/CONNECTOROctober 28, 1983
K832725DUAL DIAL VENTURI STYLE MASKSeptember 20, 1983
K831246WHISTLER IN-LINE PRESSURE RELEASE VALVEJuly 26, 1983
K830895SINGLE USE NEBULIZER, ADJUST. AIR-April 28, 1983
K830896HUMIDIFIER, WITH OR WITHOUT ADAPTERApril 18, 1983
K821129AIRLIFE NEBULIZER HEATERMay 18, 1982
K821128DISPOSABLE THERMOPLASTIC RUBBER MOUTHMay 13, 1982
K812067INSPIRATORY FORCE PRESSURE ADAPTORAugust 12, 1981
K812066PERCENTO MASK, PEDIATRIC, UNDER-THE-CHINAugust 3, 1981
K811908IMV MANIFOLDSJuly 16, 1981
K811890DISPOSABLE TRACH T OXYGENATORJuly 15, 1981
K811708UNIVERSAL ADAPTER SYSTEM-U/ADAPITJuly 1, 1981
K811711PEDIATRIC OXYGEN MASKSJuly 1, 1981
K811161HUMIDIFIER W/ OR W/OUT ADAPTORJune 24, 1981
K810946ADULT & PEDIATRIC TRACHEOSTOMY MASKSJune 2, 1981
K810947AIR ENTRAINMENT TRACH TJune 2, 1981