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 48 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 Celebrities back Function in $53M Series A funding round Pilots - June 26, 2024 0 Roundup: Lunit INSIGHT CXR comes to Brazil and more briefs Pilots - January 6, 2023 0 Butterfly Network reports over $33M loss in Q1 Pilots - May 12, 2023 0 Q&A: Wellth’s new chief operating officer on his plans for the company Pilots - September 27, 2024 0 Babylon Health sells majority of U.K. assets to eMed Pilots - September 5, 2023 0 POPULAR CATEGORIESPilots2166Applications750Testing283Collaborations15GitHub3