Federal Register Notice: FDA is making available a draft guidance for industry and FDA staff entitled Compliance With Section 301 of the Medical Device User Fee and Modernization Act of 2002 — Identification of Manufacturer of Medical Devices. Section 301 of the Medical Device User Fee and Modernization Act of 2002 requires that a device, or an attachment to the device, bear prominently and conspicuously the name of the manufacturer, a generally recognized abbreviation of such name, or a unique and generally recognized symbol that identifies the manufacturer. TTo download this guidance, click here. To view this notice, click here.
