For FDA approval diagnostic devices, analytical validation of the device to establish performance characteristics, such as analytical specificity, precision (repeatability and reproducibility), and limits of detection, is essential.
In conclusion, the use of consumer-targeted wearable and mobile sleep monitoring technology has largely focused on validation of devices and applications compared with polysomnography (PSG) but opportunities exist for observational research and for delivery of behavioral interventions.
Validation of device-specific 'acceptability criteria' for field applications should be a priority of future research.
An experimental validation of the device is also performed.
Several application cases are examined and used for validation of the device model.
Finally, preliminary results that provide experimental validation of the device design are presented.
This study represents the first reported validation of this device in patients as well as in vitro.
Following validation of the device, its use in biomechanical studies assessing radiocapitellar and ulnar load sharing as a function of length changes of the radius will be performed.
For validation purposes, the device was used to determine the CO present in the 4-shed accumulated smoke of two cigarette types after passing smokers' lungs.
In this paper, we present the design and implementation of S-MARKS which incorporates device validation, resource discovery and a privacy module.
Moreover, this paper presents the design of a single phase Intelligent Power Router, simulations that prove its capability to control the power flow; and finally, an experimental validation of the device operation is also offered.
