Recently the U.S. Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH) launched a new web section “Coronavirus Disease 2019 (COVID-19) Emergency Use Authori... Read more

By Airman 1st Class Dwane Young Driving past a little girl holding her mom’s hand while clinching a doll, is nothing out of the ordinary. Taking a second glance, you realize everyone is wear... Read more

In response to public health and safety concerns about the appropriateness of decontaminating certain respirators, the U.S. Food and Drug Administration (FDA) is reissuing certain Emergency... Read more

  The U.S. Food and Drug Administration announced the following actions taken in its ongoing response effort to the COVID-19 pandemic: The FDA issued an updated FDA COVID-19 Response At... Read more

COVID-19 hot spots across the nation are receiving 6,000 3D-printed face shields to protect the healthcare technology management (HTM) professionals responsible for managing and maintaining... Read more

  Royal Philips has announced that the U.S. FDA has issued an Emergency Use Authorization (EUA) for Philips’ IntelliVue Patient Monitors MX750/MX850 and its IntelliVue Active Displays A... Read more

The U.S. Food and Drug Administration today continued to take action in the ongoing response to the COVID-19 pandemic:   The FDA issued an Emergency Use Authorization for the Stryker Su... Read more

The U.S. Food and Drug Administration today announced the following actions taken in its ongoing response effort to the COVID-19 pandemic: The FDA issued an Emergency Use Authorization (EUA)... Read more

On May 21, 2020, the U.S. Food and Drug Administration (FDA) issued a guidance to help foster continued availability of medical devices during the COVID-19 public health emergency. Per the g... Read more

U.S. PIRG delivered a letter to congressional lawmakers on Monday, signed by 326 hospital repair experts, calling for manufacturers to stop withholding what technicians need to fix medical e... Read more