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 47 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 Akili Interactive announces board nominees ahead of SPAC and more digital health hires Pilots - July 11, 2022 0 Happify Health partners with Biogen on multiple sclerosis patient engagement tool Pilots - June 23, 2022 0 Q&A: How ambient documentation is altering the provider workload Pilots - December 29, 2022 0 At-home diagnostics company LetsGetChecked wraps up BioIQ acquisition Pilots - May 3, 2022 0 eHealth Ventures raises $30 million for digital health fund Pilots - January 25, 2022 0 POPULAR CATEGORIESPilots2166Applications750Testing283Collaborations15GitHub3