Trek Diagnostic Systems, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trek Diagnostic Systems, Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Trek Diagnostic Systems, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Historical record: 7 cleared submissions from 2004 to 2011. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Trek Diagnostic Systems, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trek Diagnostic Systems, Ltd.
7 devices
Cleared
Sep 22, 2011
SENSITITRE OPTIREAD
Microbiology
205d
Cleared
Aug 18, 2011
SENSITITRE (R) HP MIC SUSCEPTIBILITY PLATE WITH CEFAROLINE (0.004-8UG/ML) AND...
Microbiology
87d
Cleared
Apr 27, 2011
SENSITITRE AIM (TM)
Microbiology
83d
Cleared
Feb 25, 2010
SENSITIVE HAEMOPHILUS INFLUENZAE, STREPTOCOCCUS PNEUMONIA, (HP) MIC...
Microbiology
83d
Cleared
Dec 16, 2009
SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES
Microbiology
128d
Cleared
Oct 13, 2006
SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
Microbiology
35d
Cleared
Jul 27, 2004
SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC SUSCEPTIBILITY PLATE...
Microbiology
49d