FDA 510(k) Applications Submitted by AMEDITECH, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K113501 11/25/2011 AMEDITECH CHECKCUP MULTI DRUG TEST (FLAT/ROUND CUP) AMEDITECH, INC.
K113046 10/13/2011 AMEDITECH IMMUTEST MILTI-DRUG SCREEN AMEDITECH, INC.
K040092 01/16/2004 AMEDITECH IMMU TEST DRUG SCREEN PANEL AMEDITECH, INC.
K050186 01/27/2005 AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III AMEDITECH, INC.
K011813 06/11/2001 AMEDITECH IMMUTEST DRUG SCREEN THC AMEDITECH, INC.
K011814 06/11/2001 AMEDITECH IMMUTEST DRUG SCREEN COC AMEDITECH, INC.
K012483 08/02/2001 AMEDITECH IMMUTEST DRUG SCREEN OPIATES AMEDITECH, INC.
K012484 08/02/2001 AMEDITECH IMMUTEST DRUG SCREEN AMPHETAMINE AMEDITECH, INC.
K012582 08/10/2001 AMEDITECH IMMUTEST DRUG SCREEN PCP AMEDITECH, INC.
K012585 08/10/2001 AMEDITECH IMMUTEST DRUG SCREEN METHAMPHETAMINE AMEDITECH, INC.
K023126 09/19/2002 AMEDITECH IMMUTEST HCG PREGANCY TEST AMEDITECH, INC.
K063015 10/02/2006 AMEDITECH IMMUTEST MULTI-DRUG SCREEN BUP/PPX/COC150 AMEDITECH, INC.
K042975 10/28/2004 AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL II AMEDITECH, INC.
K053175 11/14/2005 AMEDITECH DRUGSMARTCUP AMEDITECH, INC.


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