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AlertWatch:OR and AlertWatch:OB are FDA 510(k)-cleared for sale in the United States, and are intended for use by clinicians for secondary monitoring of patients . AlertWatch accomplishes this by aggregating data from a multitude of sources and displaying them at a central location. Once alerted, the clinician must refer to the primary monitoring device before making a clinical decision.
AlertWatch:ICU, AlertWatch:AC, and AlertWatch:PACU are pending FDA clearance and are currently only available for IRB-sponsored research. Some images and interfaces are enhanced for clarity.