Sep 30, 2019 · CDR Kimberly Piermatteo, MHA Consumer Safety Officer Division of Industry and Consumer Education Office of Communication and Education Center for Devices and Radiological …

Feb 24, 2021 · In response to the National Strategy, the Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) led an effort to develop recommendations for device types …

The following device specifications are not required but are strongly recommended based on what best supports student success in a digital learning environment.

This form collects opinions and observations from dental health care personnel (DHCP) who have pilot tested a safer dental device. This form can be adapted for use with multiple types of safer devices.

May 19, 2025 · Finding Medical Device and Drug Approval Information Through the Food and Drug Administration Databases The U.S. Food and Drug Administration (FDA) maintains a variety of …

FDI device packages include a device description, an optional User Interface Plug-in (UIP) providing a rich graphical user interface for more sophisticated device applications, and attachments which can …

When the use of a device or implant is necessary in the performance of certain procedures, the device or implant must be submitted with the same date of service and on the same claim as the procedure.