center4research.org NCHR testimony at 2016 FDA meeting on the classification of ... NCHR testimony at 2016 FDA meeting on the classification of ... 1 Mar 2016 ... NCHR testimony at 2016 FDA meeting on the classification of ... FDA Advisory Committee Meeting on Reclassification of Urogynecologic Surgical Mesh Instrumentation and Classification of Separator, automated, blood cell and plasma, ... Currently, surgical mesh instrumentation is listed as a class I device., center4research.org Testimony, Briefings, Statements,
Patient, Consumer, and Public Health Coalition testimony at 2016 FDA public meeting on demographic subgroup data