DURECT Announces Filing of Special 510(k) Application for its New Generation IntraEAR(R) Ear Catheter Product and Approval of Physician Sponsored Investigational New Drug Application for Treatment …
CUPERTINO, Calif., June 25 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) announced today that it has filed a Special 510(k) pre-market notification with the FDA for its next generation ear delivery catheter. Like its predecessor IntraEAR(R) catheters, the Microdose Cath(TM) is intended for the site-directed delivery of fluids to the round window area of the middle […]