Philips launches Duo venous stent system with FDA approval
Philips (NYSE: PHG) today announced the first implant of its Duo venous stent system following FDA premarket approval.
Philips (NYSE: PHG) today announced the first implant of its Duo venous stent system following FDA premarket approval.
Getinge announced today that it received FDA 510(k) clearance for its Talis +ACG (advanced clinical guidance) support software.
Medical imaging AI company receives approval for algorithm enabling opportunistic detection and triage of vertebral compression fractures.
Challenge Works today announces that Sysmex Astrego’s PA-100 AST System has won the $10m (£8m) Longitude Prize on AMR.