The legislation also calls for the FDA to produce a report on the quality and safety of devices with respect to servicing within 270 days of enactment. Currently, only medical device service activities performed by a manufacturer are regulated by the FDA.
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Technical Prospects has received ISO 9001:2015 certification for the disassembly, repair, refurbishment, quality assurance, technical support, and technical training of…
Samsung introduced the HS50 and HS60 ultrasound systems in May at the American College of Obstetricians and Gynecologists annual meeting…
Demand for quality used parts has increased as hospitals and health care systems have become more sophisticated about medical equipment…
The ProbeHunter team, the Scandinavian-developed system for quality assurance of ultrasound probes, has announced that the business is expanding. Imaging…
FUJIFILM Medical Systems U.S.A. Inc. has announced that its Synapse Mobility Enterprise Web Viewer has been granted Authority to Operate…
The Webinar Wednesday series continues to receive rave reviews and reach new highs as more and more people in the…
KUBTEC has announced that the U.S. Patent Office has granted the company an additional patent for its technology used for…
Richardson Electronics Ltd. has announced the sale of its picture archiving and communication systems (PACS) display business, including the Image…
BC Group International Inc. and RTI Electronics Inc. have announced a partnership between the two organizations for the distribution of…
