FDA Clears Enhanced Microbial Identification System Features
New clearances expand MALDI-TOF platform capabilities with improved software, faster sample prep, and broader species coverage.
New clearances expand MALDI-TOF platform capabilities with improved software, faster sample prep, and broader species coverage.
Avails Medical, a developer of antibiotic susceptibility testing tech, received 510(k) clearance from the U.S. FDA for its new eQUANT system.Â
Magnolia Medical Technologies shared a study detailing the clinical and financial impacts of blood culture contamination on patient safety.
This method of fluorescence microscopy for cell observation circumvents fundamental problems: light-induced destruction and unceasing molecule movement.
BD received FDA 510(k) clearance for the BD Kiestra IdentifA system, which automates the preparation of bacterial identification testing.
The era of space exploration brings with it a new risk: invasion. But not from little green men, rather, from microbiological contamination.
Hardy Diagnostics has released its latest chromogenic media, HardyCHROM Group A Strep agar, for selective cultivation of clinical specimens.