FDA Device Clearances: Neurostimulation Lead, Power Injectable Ports and Safety Needles, Automated Blood Testing Instrument

The US Food and Drug Administration has granted premarket approval for a neurostimulation lead, 510(k) clearance for power injectable ports and safety needles, and an automated blood testing instrument.Jill Taylor

Continue to FDA Device Clearances: Neurostimulation Lead, Power Injectable Ports and Safety Needles, Automated Blood Testing Instrument on Medscape Medical News Headlines.

Medical Buzz delivers the most recent headlines from the medical world. Diseases, cures, accidents, medicin. Click below for more headlines ...
Medical buzz