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Standards for nanomaterials and cardiac valve prostheses make the grade in US

This article was originally published in SRA

Executive Summary

The US Food and Drug Administration has made 20 new entries to its list of recognized medical device standards for use in pre-market reviews1. Other changes to the list include the withdrawal of standards and their replacement by others where applicable, correction of errors in previously recognized standards, and changes to the supplementary information sheets of recognized standards that describe revisions to the applicability of the standards.

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