cobas eplex respiratory pathogen panel 3
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Roche receives FDA 510(k) clearance for new cobas eplex respiratory pathogen panel 3
Roche announced the FDA 510(k) clearance of the cobas eplex respiratory pathogen panel 3 (RP3), a flexible syndromic test that detects up to 19 viral and bacterial targets from a single nasopharyngeal swab. The panel offers up to five customizable configurations, requires less than one minute of hands-on time, and delivers results in under two hours.