Home » FDA Clears Respiratory Virus Identification Kit
FDA Clears Respiratory Virus Identification Kit
Diagnostic Hybrids, a leading developer of IVD fluorescent staining kits and cell culture products, announced the FDA 510k clearance of its D3 FastPoint L-DFA Respiratory Virus Identification Kit, which allows the individual detection of influenza A, influenza B, respiratory syncytial virus, human metapneumovirus, adenovirus and parainfluenza viruses from a patient’s specimen in under 30 minutes.
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