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Kentron Health Care, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
5
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K030693KENTEX DISPOSABLE VAGINAL SPECULUMAugust 27, 2003
K971917KENTRON'S ISOLATION GOWNSeptember 19, 1997
K972410IMPERVIOUS ISOLATION GOWNSeptember 19, 1997
K953465KENTEMPDecember 15, 1995
K953914KENTEXNovember 6, 1995
K953830KENSORBOctober 3, 1995