ReddyPort Elbow Device Gets FDA Clearance July 27, 2023 by Laurie Watanabe The ReddyPort elbow device used for non-invasive ventilation (NIV) has received 510(k) premarket clearance from the U.S. Food & Drug Administration. -->
CGS: Authentication Policies to Change in February Going forward, providers will need to use the Computer Telephone Integration system for claims or eligibility issues.
CMS Releases Details of Lymphedema Compression Treatment Coverage Medicare coverage starts Jan. 1, 2024.
HME Business “Insight Issue” Highlights New Product Award Winners Industry leaders share their perspectives on 2023 as they look ahead to the new year.