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Vabar Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K790749COLOSTOMY ENEMA DEVICEMay 16, 1979
K790750COLOSTOMY DEVICE W/ PRESSURE LIDMay 14, 1979