Trinity Biotech - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Trinity Biotech has 5 FDA 510(k) cleared medical devices. Based in Jamestown, US.
Historical record: 5 cleared submissions from 2009 to 2017. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Trinity Biotech Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trinity Biotech
5 devices
Cleared
Oct 23, 2017
Lyme B. burgdorferi (IgM) MarStripe Test
Microbiology
89d
Cleared
Feb 01, 2017
Lyme B. burgdorferi (IgG) MarStripe Test
Microbiology
89d
Cleared
Mar 01, 2013
UNIGOLD GIARDIA
Microbiology
423d
Cleared
Feb 08, 2013
UNI-GOLD CRYPTOSPORIDIUM
Microbiology
255d
Cleared
Jul 02, 2009
DESTINY MAX COAGULATION ANALYZER
Hematology
185d