Heartstream Forerunner AED to commence shipments in fourth quarter; product cleared Sept. 11.
This article was originally published in The Gray Sheet
Executive Summary
HEARTSTREAM FORERUNNER AED TO COMMENCE SHIPMENTS IN FOURTH QUARTER following FDA 510(k) clearance of the automatic external defibrillator Sept. 11, the firm states. Manufacturing ramp-up for the device will be relatively quick, Heartstream says, because the firm sources most of the system's components from suppliers. Heartstream performs final assembly of the Forerunner at its facilities in Seattle.