Ventrex, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K061044FEATHERLITE AQUA TOCODYNAMOMETERJuly 12, 2006
K013477TOCO LITE, MODEL TD-01January 17, 2002
K964821COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67July 16, 1997
K963415VENTREX OXYGEN SENSORNovember 25, 1996
K925044VENTREX ALLERGEN DISCMay 14, 1993
K924119VENTREX ALLERGEN DISCNovember 30, 1992