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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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