Cerner Receives FDA Clearance For Medical Device Connectivity Solution
January 13, 2010, 2010 (FinancialWire) — The Cerner (NASDAQ: CERN) CareAware iBus, a way to connect medical devices to support the entire hospital care process, recently received 510(k) pre-market clearance from the U.S. Food and Drug Administration and is now available in the United States and all U.S. territories.
The Cerner CareAware iBus solution provides plug-and-play capabilities for connecting any medical device to any EHR system. Once a device is connected to the Cerner CareAware iBus solution, it is immediately recognized and can begin transmitting data to the EHR. This connectivity architecture places the EHR at the center of all information created and stored on the patient to create a Single Source of Truth.
The solution also allows waveform data to be transmitted directly into the EHR. The Cerner CareAware iBus solution also provides the ability to correlate and trend various sources of information including various waveforms, heart rate and blood pressure. This trending information allows clinicians to analyze the patient’s data in the context of other clinically relevant data for a specific time period.
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