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Airco/Ohio Medical Products

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K833459COAXIAL VOL. VENTILATOR CIRCUITJanuary 10, 1984
K833452OHIO GMS ABSORBERNovember 29, 1983
K832418OHIO TEMPERATURE SIMULATORSeptember 12, 1983
K832565OHIO 5400 VOLUME MONITORSeptember 1, 1983
K832185OHIO MODEL 922 SPIROMETERAugust 12, 1983
K830446OXYGEN MONITOR OHIO 5100March 24, 1983
K822456OHIO V5A ANESTHESIA VENTILATORSeptember 21, 1982
K813476OHIO VOLUME INCENTIVE SPIROMETERDecember 31, 1981
K812879OHIO NON-REUSABLE TRACHEAL TUBE MURPHYNovember 24, 1981
K812880OHIO NON-REUSABLE TRACHEAL TUBE MAJILLNovember 24, 1981
K811413DABC NONCONDUCTIVE PEDIAT. ANESTH. CIRJune 2, 1981
K810763OHIO DISPOSABLE TRACHEAL TUBEMarch 27, 1981
K790809VS, ANESTHESIA VENTILATORMay 4, 1979