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Khi, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K830404RAD VALVEMarch 17, 1983
K830399COUPLING/VALVEMarch 10, 1983
K811858KHI CPRAM BREATHING CIRCUITJuly 16, 1981
K800456EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.March 18, 1980