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Kmi Diagnostics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K010790
CORTISOL LIA
January 29, 2002
K990073
CALCITONIN
May 11, 1999
K973900
TESTOTERONE ELISA
February 24, 1998
K973901
17 B-ESTRADIOL (ELISA)
November 24, 1997
K973898
PROGESTERONE ELISA
November 13, 1997
K973897
DHEA-S
November 13, 1997