We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » FDA Notes MDR Issues in Form 483 to Avinger
FDA Notes MDR Issues in Form 483 to Avinger
May 5, 2011
Avinger has received a Form 483 for failing to submit a medical device report (MDR) to the FDA after receiving information suggesting one of its devices may have led to patient injury.