FDA-ISO-10993 › Historical Revision Information
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
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
2013 DRAFT
Status
Superseded
Publication Date
April 23, 2013
Page Count
38 pages