Summary:
«MESI mTABLET ABI, a device used for early detection of Peripheral Arterial Disease (PAD) by measuring Ankle-Brachial Index (ABI), was cleared for marketing and sales by the Food and Drug Administration in December 2020. MESI mTABLET ABI is a unique healthcare solution, integrating wireless diagnostic modules for Ankle-Brachial Index measurement, patient records, and medical apps in one system. The FDA’s decision means that healthcare professionals in the USA will get access to the latest medical technology allowing more patients to be diagnosed with Peripheral Arterial Disease, a cardio-vascular disease with severe consequences, earlier.»
Article written by Health Tech Digital
26|01|2021
Source:
Health Tech Digital