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FDA 510(k) Applications Submitted by JAMES H 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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