Reusable Menstrual Pads Classified As Medical Devices
Retailers are being required to pay a “premarket notification fee” to continue the sale of Reusable Menstrual Pads. Because the Food and Drug Administration (FDA) classifies menstrual cups and reusable menstrual pads as “medical devices,” retailers are being required to pay a “premarket notification fee” to continue the sale of … [Read more...] about Reusable Menstrual Pads Classified As Medical Devices
Transvaginal Mesh for POP Repair Should be Classified
Classification of Transvaginal Mesh Pop Repair An advisory panel for the U.S. Food & Drug Administration (FDA) voiced support for an agency proposal to reclassify transvaginal mesh devices used to repair pelvic organ prolapse (POP) as high risk, or Class III. If the FDA does go forward with the change, manufacturers of would … [Read more...] about Transvaginal Mesh for POP Repair Should be Classified
