Ingrid Nygaard. Show Affiliations »
Abstract
Mesh: See more » Device Approval/legislation & jurisprudenceDevice Approval/standardsEquipment FailureFemaleGynecologyHumansMandatory ReportingObstetricsUnited StatesUnited States Food and Drug Administration
Year: 2008 PMID: 18165386 DOI: 10.1097/01.AOG.0000298949.87683.b2
Source DB: PubMed Journal: Obstet Gynecol ISSN: 0029-7844 Impact factor: 7.661