Pro-Lab, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PROLEX (STREPTOCCAL GROUPING LATEX KIT), AMNIOTEST(TM), LEGIONELLA REAGENS FOR DIRECT FLUORESCENT ANTIBODY
27
Total
26
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pro-Lab, Inc. Chemistry ✕
1 devices