Pro-Lab Diagnostics is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Pro-Lab Diagnostics - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pro-Lab Diagnostics has 5 FDA 510(k) cleared medical devices. Based in Ontario, CA.
Historical record: 5 cleared submissions from 1992 to 1994. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Pro-Lab Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pro-Lab Diagnostics
5 devices
Cleared
Dec 15, 1994
E.COLI 0157 LATEX TEST
Microbiology
119d
Cleared
Dec 24, 1992
TRANSYSTEM LIQUID AMIES MEDIUM
Microbiology
119d
Cleared
Dec 24, 1992
TRANSYSTEM AMIES W/O CHARCOAL
Microbiology
119d
Cleared
Dec 24, 1992
TRANSYSTEM AMIES WITH CHARCOAL
Microbiology
119d
Cleared
Dec 24, 1992
TRANSYSTEM LIQUID STUART MEDIUM
Microbiology
119d