FDA 510(k) Applications Submitted by JAMES L BROWN

FDA 510(k) Number Submission Date Device Name Applicant
K971336 04/10/1997 CAIRD TECHNOLOGY SPIROMETER CAIRD TECHNOLOGY
K101016 04/12/2010 ANS SYSTEM CAIRD TECHNOLOGY
K012686 08/14/2001 CAIRD TECHNOLOGY HOLTER 2000 CAIRD TECHNOLOGY
K962306 06/17/1996 FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES DIAGNOSTIC HYBRIDS, INC.
K972414 06/27/1997 FRESHCELLS DIAGNOSTIC HYBRIDS, INC.
K962780 07/17/1996 FRESHCELLS, HEP-2 DIAGNOSTIC HYBRIDS, INC.
K962782 07/17/1996 FRESHFROZEN CELLS, HEP-2 DIAGNOSTIC HYBRIDS, INC.
K022713 08/14/2002 DFA RESPIRATORY VIRUS SCREENING & ID KIT DIAGNOSTIC HYBRIDS, INC.


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