FDA clarifies multiple-function medical device oversight policy

This article was originally published here

By Stewart Eisenhart, Emergo Group

New guidance from the US Food and Drug Administration addresses premarket authorization requirements for multiple-function products with at least one function that qualifies as a medical device.

Get the full story here at the Emergo Group’s blog.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.

The post FDA clarifies multiple-function medical device oversight policy appeared first on MassDevice.

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