FDA 510(k) Applications Submitted by DAVID M LYERLY, PH.D.

FDA 510(k) Number Submission Date Device Name Applicant
K030704 03/06/2003 IBD-QUIK CHEK TECHLAB, INC.
K030991 03/28/2003 C. DIFF CHEK - 30 TECHLAB, INC.
K030992 03/28/2003 C. DIFF CHEK - 60 TECHLAB, INC.
K971182 03/31/1997 TOX A/B TEST TECHLAB, INC.
K050891 04/08/2005 TOX A/B QUICK CHEK TECHLAB, INC.
K011396 05/07/2001 IBD-CHEK TECHLAB, INC.
K051927 07/18/2005 TECHLAB ASCA-CHEK TECHLAB, INC.
K042071 08/02/2004 IBD-SCAN TECHLAB, INC.
K033274 10/10/2003 GIARDIA II TECHLAB, INC.
K052932 10/19/2005 CRYPTOSPORIDIUM II TECHLAB, INC.
K003306 10/20/2000 C. DIFFICILE TOX A/B II TECHLAB, INC.
K994101 12/06/1999 E. HISTOLYTICA II TECHLAB, INC.
K053572 12/22/2005 C. DIFF QUIK CHEK TECHLAB, INC.
K955895 12/26/1995 E. HISTOLYTICA TEST TECHLAB, INC.
K955897 12/26/1995 CRYPTO/GIARDIA-CEL IF TEST TECHLAB, INC.
K980354 01/29/1998 CRYPTOSPORIDIUM TEST TECHLAB, INC.
K963135 08/12/1996 GIARDIA CELISA TECHLAB, INC.
K955852 12/26/1995 CRYPTO-CEL IF TEST TECHLAB, INC.


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