FDA 510(k) Applications Submitted by MARK A KOWAL

FDA 510(k) Number Submission Date Device Name Applicant
K010790 03/15/2001 CORTISOL LIA KMI DIAGNOSTICS, INC.
K973897 10/14/1997 DHEA-S KMI DIAGNOSTICS, INC.
K973898 10/14/1997 PROGESTERONE ELISA KMI DIAGNOSTICS, INC.
K973900 10/14/1997 TESTOTERONE ELISA KMI DIAGNOSTICS, INC.
K973901 10/14/1997 17 B-ESTRADIOL (ELISA) KMI DIAGNOSTICS, INC.


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