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FDA Finalizes Guidance on RF in Wireless Medical Devices

On August 14, 2013, the Food and Drug Administration released the final guidance titled “Radio Frequency Wireless Technology in Medical Devices” for incorporating and integrating RF wireless technology in medical devices. 

The guidance covers devices that are worn on the body or implanted and others that are intended for use in locations such as hospitals, clinics and clinical laboratories. The draft guidance was originally issued in January 2007 (72 Fed. Reg. 137).

The guidance discusses issues for the effective use of medical devices that incorporate RF wireless technology including how to select wireless technology, the quality of service, coexistence, security and electromagnetic compatibility. Manufacturers of medical devices are recommended to address potential issues related to the incorporation of RF wireless technology that may affect the safe and effective use of these type of devices.

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Common Test & Calibration Uses of a Portable Signal Generator in The Field

This versatile field device generates signals that mimic various sensors to test and calibrate equipment. It helps technicians troubleshoot connections and verify system performance. Portable and battery-powered, it's designed for on-site diagnostic work in industrial environments.

Read the guidance “Radio Frequency Wireless Technology in Medical Devices” in detail on the Food and Drug Administration’s website. 

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