Nasdaq

bioMérieux receives FDA 510(k) Clearance for its VITEK® COMPACT PRO, a new ID/AST system to fight against antimicrobial resistance

MARCY L'ÉTOILE, France, March 18, 2025 /PRNewswire/ --bioMérieux, a world leader in the field of in vitro diagnostics, announces the U.S. Food and Drug Administration (FDA) 510(k) clearance for VITEK® ...
WTNH

Colibrí™, COPAN's Automated Specimen Workup Instrument, Receives FDA 510(k) Clearance for use with bioMérieux VITEK® 2 Antimicrobial Susceptibility Testing (AST) System

Colibrí™, COPAN's Automated Specimen Workup Instrument, Receives FDA 510 (k) Clearance for use with bioMérieux VITEK® 2 Antimicrobial Susceptibility Testing (AST) System News provided by COPAN ...
KOLR10 & Ozarks Local News

Colibrí™, COPAN's Automated Specimen Workup Instrument, Receives FDA 510(k) Clearance for use with bioMérieux VITEK® 2 Antimicrobial Susceptibility Testing (AST) System

This same instrument has now received its second FDA 510 (k) clearance for the preparation of microbial suspensions for AST with bioMérieux VITEK 2, making Colibrí™ the first instrument in its class ...