Hospira Receives FDA 510(k) Clearance for Plum 360™ Infusion System

by PRNewsire

LAKE FOREST, Ill., Jan. 20, 2015 /PRNewswire/ -- Hospira, Inc. (NYSE:  HSP), the world's leading provider of injectable drugs and infusion technologies, today announced that the company has received 510(k) regulatory clearance from the U.S. Food and Drug Administration (FDA) for the Plum 360™ infusion system with Hospira MedNet™ safety software. The newest in Hospira's portfolio of infusion devices, the Plum 360 system builds on the unique air management and secondary delivery features of Plum A+™, while expanding its drug library and wireless capability to enable streamlined electronic medical record (EMR) integration.

See the full article here.

Go to kBLASTER to FDA 510(k) search for a primary predicate, multiple predicates or reference devices, and harness kBLASTER's uniquely effective result management features, so you can quickly build a successful 510(k) clearance strategy.