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Broadwest Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K864499PODOSCOPEFebruary 4, 1987
K864569PODODIGITALFebruary 4, 1987
K852302INOX IORCEPS JARJuly 2, 1985
K852301INOX THERMOMETER JARJuly 1, 1985
K852300INOX IV STANDJune 20, 1985
K851307INOX DRY HEAT STERILIZERMay 9, 1985