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Kmi Diagnostics, Inc.

FDA Regulatory Profile

Kmi Diagnostics, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 29, 2002.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K010790CORTISOL LIAJanuary 29, 2002
K990073CALCITONINMay 11, 1999
K973900TESTOTERONE ELISAFebruary 24, 1998
K97390117 B-ESTRADIOL (ELISA)November 24, 1997
K973898PROGESTERONE ELISANovember 13, 1997
K973897DHEA-SNovember 13, 1997

FDA data resources