Roche announced has obtained 510(k) clearance from the US Food and Drug Administration (FDA) for the use of four additional specimen types with the cobas CT/NG v2.0 test to help physicians diagnose Chlamydia trachomatis (CT) and Neisseria ...
The US Food and Drug Administration (FDA) has approved Roche's new streamlined workflow process for the cobas Human Papillomavirus (HPV) Test, which help labs reduce costs, improve turnaround time and focus on other key tasks. Roche ...
Tags: Cobas HPV Test, FDA Approval, Medicine