FDA-PATIENT-PREFER Complete Document History
Patient Preference Information - Voluntary Submission, Review in Premarket Approval Applications, Humanitarian Device Exemption Applications, and De Novo Requests, and Inclusion in Decision Summaries and Device Labeling - Guidance for Industry, Food and Drug Administration Staff, and Other Stakeholders

Complete Current Edition:
   2016 EDITION - Guidance for Industry, Food and Drug Administration Staff, a - Aug. 24, 2016

Obsolete Revision Information:
   2015 DRAFT - Draft Guidance for Industry, Food and Drug Administration St - May 14, 2015