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Bruel & Kjaer

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K925484CARBON DIOXIDE & OXYGEN MONITOR TYPE 1308June 22, 1993
K914295ANESTHETIC GAS MONITOR TYPE 1304, MODIFIEDApril 10, 1992
K905198DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535August 28, 1991
K911348RIGID ENDOSCOPEJune 21, 1991