CDRH

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CDRH

(Center for Devices and Radiological Health) A branch of the U.S. Food and Drug Administration that governs medical devices as well as non-medical devices that emit radiation, such as cellphones.

Classes 3, 2 and 1
Class 3 devices are the most critical and must go through rigorous testing before approval, similar to pharmaceutical drugs. Class 2 devices are considered low risk, and manufacturers go through a less rigorous "510k" approval process for new models that are similar to existing products. However, a report released in 2011 by the National Research Center for Women and Families and the Cleveland Clinic showed that several 510k-approved devices in the previous five years had caused serious health problems when they failed to operate properly. Class 1 devices are harmless to users if they fail to operate. See healthcare IT.
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He served as the Secretary General of the CDHR which is composed of a consortium of over fifty-five organizations working together to champion the rights of minorities living in Islamic countries.
8 [greater than or equal to]30% (a) Values are mean (SD) except for 10-year CDHR, which is given as median (interquartile range).
From technology expertise to a national network of state clients, MAXIMUS gives CDHR the tools needed for us to grow," stated David Richardson.