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 | Document Center, Inc.

FDA-ISO-10993 › Complete Document History
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

Complete Current Edition:

2020 EDITION - Use of International Standard ISO 10993-1 - Sept. 4, 2020

Obsolete Revision Information:

2016 EDITION - Guidance for Industry and Food and Drug Administration Staff - June 16, 2016
2013 DRAFT - Draft Guidance for Industry and Food and Drug Administration - April 23, 2013