FDA-ISO-10993 › Use of International Standard ISO 10993-1, 'Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process' - Guidance for Industry and Food and Drug Administration Staff

FDA-ISO-10993 - 2020 EDITION - CURRENT
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Use of International Standard ISO 10993-1, 'Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process' - Guidance for Industry and Food and Drug Administration Staff


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Document Number

FDA-ISO-10993

Revision Level

2020 EDITION

Status

Current

Publication Date

Sept. 4, 2020

Page Count

68 pages