- The FDA has granted 510(k) clearance to Becton, Dickinson And Company's BDX BD Kiestra Methicillin-resistant Staphylococcus aureus (MRSA) imaging application.
- Staphylococcus aureus is a bacteria that causes various clinical diseases with potentially serious infections. BD Kiestra uses artificial intelligence software to interpret bacterial growth and release negative specimens.
- The imaging application automatically organizes specimens in meaningful worklists with minimal human interaction, enhancing microbiology laboratory efficiency and workflow.
- Also Read: Becton, Dickinson Shares Dip Despite Q2 Earnings Beat - Here Are The Details
- The FDA nod will enable medical laboratory scientists and technicians to spend more time on higher-value analysis, reducing the administrative burden on technicians.
- The application can evaluate single specimens or group together a large volume of plates.
- "The pandemic created significant and ongoing labor challenges in laboratories, and reading plates is a labor-intense, potentially error-prone process in microbiology," said Nikos Pavlidis, vice president and general manager for Diagnostics at BD.
- Price Action: BDX shares are up by 0.17% to $251.50 in premarket on the last check Tuesday.
- Photo Via Company
BDXBecton Dickinson & Co
$201.781.34%
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