MiniBox+ Cleared for Sale in the USA

MiniBox+ Cleared for Sale in the USA

PulmOne Advanced Medical Devices is pleased to announce that the U.S. Food and Drug Administration (FDA) has cleared the MiniBox+ device for sale in the USA. In addition to all the parameters measured by the MiniBox, the MiniBox+ has an integrated module for single breath Carbon Monoxide Diffusing Capacity (DLCO) testing. It offers fully automated measurements of Calculated DLCO, VA, and KCO.

With this clearance, PulmOne now offers complete pulmonary function testing in any clinical setting.