U.S. Rep. Scott A. Peters (D-California) is attempting to define "remanufacturing" when it comes to medical devices via H.R. 7253. "Remanufacturing" is a term that has befuddled healthcare technology management (HTM) professionals, original equipment manufacturers (OEMs), the FDA and other stakeholders for at least half a decade. H.R. 7253 appears to offer changes to 21 USC 360: Registration of producers of drugs or devices.
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