The John Bunn Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
20
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K900854JOHN BUNN: MEDIX COMPACT TRAVELLERApril 23, 1990
K883216BUNN MODEL 50 OXYGEN FLOW CONTROLLERAugust 18, 1988
K873071BUNN CONCENTRATOR MODEL 2100 SERIESSeptember 15, 1987
K870094BUNN MODEL 530 ASPIRATORMarch 6, 1987
K861435BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVENovember 7, 1986
K861199BUNN MODEL 22 OXYGEN FLOW CONTROLLERAugust 26, 1986
K862628BUNN MODEL 510 MEDICATION COMPRESSORAugust 7, 1986
K855208BUNN LITE OXYGEN CONCENTRATORFebruary 21, 1986
K860060RX02 PLUS OXYGEN CONCENTRATORFebruary 5, 1986
K843811BUNN 3001 OXYGEN CONCENTRATOROctober 4, 1984
K841102BUNN 1000 OXYGEN CONCENTRATORApril 13, 1984
K840534LIQUID OXYGEN SYSTEMMarch 2, 1984
K821823I.V. SENTINELAugust 16, 1982
K800546BUNN VOLUMAIRE RESPIRATORY EXERCISERMarch 25, 1980
K790370BUNN MODEL #40 LOW PRESSURE ALARMMarch 28, 1979
K780863MODEL 65 HIGH & LOW PRESSURE ALARMAugust 21, 1978
K780862MODEL 290 OXYGEN RICH AIR SUPPLY UNITAugust 14, 1978
K781213COMPRESSOR, AIR, MINI-SILENTJuly 27, 1978
K761260ARIZONA OXYGEN TIMER DEVICEDecember 16, 1976
K760705OXYGEN-RICHOctober 5, 1976