1. Medical devices: cancer risk led FDA to warn against certain uses of power morcellators and recommend new labeling : report to Congressional requesters Publication: Washington, D.C. : U.S. Government Accountability Office, February 2017 Subject(s): Device ApprovalEquipment SafetyMorcellation -- adverse effectsMorcellation -- instrumentationProduct LabelingLeiomyoma -- surgeryUterine Neoplasms -- surgeryHumansUnited StatesUnited States. Food and Drug Administration
2. Non-clinical performance assessment of tissue containment systems used during power morcellation procedures: guidance for industry and Food and Drug Administration staff Publication: [Silver Spring, MD] : Center for Devices and Radiological Health, May 26, 2023 Subject(s): Device ApprovalGovernment RegulationMorcellation -- instrumentationMorcellation -- legislation & jurisprudenceMorcellation -- standardsUnited States
