From Concept To Cure, How To Secure FDA Approvals on Preclinical Medical Device Testing.
Preclinical medical device testing: how do you know you are ready and how do you make the most efficient investment in preclinical?
Surefire Precision gains FDA 510(k) clearance twice as fast as the industry average with T3 Labs
Surefire Medical achieves FDA 510(k) clearance for direct-to-tumor embolization device Surefire Precision in just 76 days with the help of T3 Labs.