Zoll medical canada evaluated the device and the device performed to specification.The device was put through extensive testing including functional testing, defib/pacer stress testing, bench handling, and defib cycling without duplicating the report.The device was recertified and returned to the customer review of the clinical logs showed the device performed a total of 6 analyses on the event date.Out of 6, the device advised shock for 2 analyses.The device identified two of the three analysis segments as shockable rhythm in both analyses and the device advised shock.The device works as expected within the limitations of the technology.This claim has been closed as device meets specification.Analysis of reports of this type has not identified an increase in trend.
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