Obstetrics and gynecology
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Obstetrics and gynecology · Oct 2012
Minimally invasive endometrial ablation device complications and use outside of the manufacturers' instructions.
To review the U.S. Food and Drug Administration (FDA) Manufacturer and User Facility Device Experience database for reports describing serious adverse events and adverse events reports describing use outside of the manufacturers' labeled instructions for the five FDA-approved minimally invasive endometrial ablation devices. ⋯ III.