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Humi Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K841682UTERINE INJECTOR 4.0MMJuly 3, 1984
K841681UTERINE MANIPULATOR 4.5MMApril 23, 1984