FDA grants 510(k) clearance to Viz.ai’s Viz Subdural Plus module
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Viz.ai for its Viz Subdural Plus module. The post FDA grants 510(k) clearance to Viz.ai’s Viz Subdural Plus module appeared first on Medical Device Network.
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Viz.ai for its Viz Subdural Plus module.
The post FDA grants 510(k) clearance to Viz.ai’s Viz Subdural Plus module appeared first on Medical Device Network.
