DEVICE APPROVAL
\dɪvˈa͡ɪs ɐpɹˈuːvə͡l], \dɪvˈaɪs ɐpɹˈuːvəl], \d_ɪ_v_ˈaɪ_s ɐ_p_ɹ_ˈuː_v_əl]\
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Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA.
By DataStellar Co., Ltd
