Is the decision to submit a 510(k) application versus a Premarket Application (PMA) at the sole discretion of a medical device manufacturer? The answer is not always clear to product liability lawyers, judges, and juries. FDA...more
By the time the COVID-19 pandemic began, society was well into the so-called “Digital Age,” relying heavily on electronic communications, apps, websites, and the like to go about daily activities. Everything from ordering...more
11/24/2021
/ Consumer Fraud ,
Coronavirus/COVID-19 ,
Electronic Communications ,
Failure To Warn ,
Food and Drug Administration (FDA) ,
Manufacturers ,
Medical Devices ,
Medical Supplies ,
Over The Counter Drugs (OTC) ,
Prescription Drugs ,
Product Safety Labels ,
QR Codes ,
Regulatory Standards ,
Vaccinations