AAA Endovascular Graft Patient Imaging Follow-Up Recommended By FDA
The Center for Devices and Radiological Health is considering a postmarket surveillance study for abdominal aortic aneurysm devices under Sec. 522 of the Safe Medical Devices Act.
The Center for Devices and Radiological Health is considering a postmarket surveillance study for abdominal aortic aneurysm devices under Sec. 522 of the Safe Medical Devices Act.