Trek Diagnostic Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trek Diagnostic Systems, Inc. - FDA 510(k) Cleared Devices
56
Total
56
Cleared
0
Denied
Trek Diagnostic Systems, Inc. has 56 FDA 510(k) cleared microbiology devices. Based in Westlake, US.
Historical record: 56 cleared submissions from 1998 to 2010.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trek Diagnostic Systems, Inc.
56 devices
Cleared
Feb 17, 2010
SENSITITRE 18-24HR SUSCEPTIBILITY PLATES
Microbiology
63d
Cleared
Jun 04, 2009
SENSITITRE YEASTONE SUSCEPTIBILITY PLATES
Microbiology
59d
Cleared
Mar 24, 2009
SENSITITRE 18-24 HOUR SUSECEPTIBILITY PLATES
Microbiology
109d
Cleared
Mar 06, 2009
SENSITITRE YEASTONE SUSCEPTIBILITY PLATES- ADDITIONAL ANTIMICROBICS
Microbiology
326d
Cleared
Oct 24, 2008
SENSITITRE VIZION
Microbiology
147d
Cleared
Mar 20, 2008
SENSITITRE 18 - 24 HOUR SUSCEPTIBILITY PLATE
Microbiology
85d
Cleared
Mar 13, 2008
SENSITITRE 18-24 SUSCEPTIBILITY PLATE
Microbiology
85d
Cleared
Jan 22, 2008
SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES
Microbiology
48d
Cleared
Dec 20, 2006
SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC AND SUSCEPTIBILITY...
Microbiology
89d
Cleared
Nov 09, 2006
MODIFICATION TO SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
Microbiology
49d
Cleared
Nov 01, 2006
SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
Microbiology
42d
Cleared
Oct 26, 2006
SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
Microbiology
38d
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