Home Pilots Tasso receives FDA 510(k) for patch-like home blood collection device Pilots Tasso receives FDA 510(k) for patch-like home blood collection device By - September 14, 2022 35 0 Facebook Twitter Pinterest WhatsApp The company said the clearance will allow more pharma companies to use Tasso+ for decentralized clinical trials. RELATED ARTICLESMORE FROM AUTHOR Pilots Medtronic issues voluntary recall of MiniMed insulin pumps Pilots Hybrid primary care company Rezilient Health scores $10M Pilots Empathy Health Technologies raises $2.8M for Sober Sidekick app LEAVE A REPLY Cancel reply Please enter your comment! Please enter your name here You have entered an incorrect email address! Please enter your email address here Save my name, email, and website in this browser for the next time I comment. FOLLOW ME0FansLike0FollowersFollow0SubscribersSubscribe POPULAR ARTICLES Sydney-based medtech Echo IQ brings AI heart screening platform to the US Pilots - December 8, 2022 0 PatientPoint partners with MyHealthTeam to connect patients with online healthcare communities Pilots - September 27, 2024 0 Google to label healthcare facilities that provide abortions in search results Pilots - August 26, 2022 0 Northwell Holdings, Aegis Ventures welcome former Mayo Clinic CEO and more digital health hires Pilots - June 14, 2023 0 Insulet announces another asset acquisition and more digital health news Pilots - February 15, 2023 0 POPULAR CATEGORIESPilots2166Applications682Testing237Collaborations15GitHub3