It's basically the level at which the FDA registers the Apple watch. I think it is given Class II instead of Class III status which means it is far easier to get through the FDA. The sensor is the piece that needs the full FDA review.As smartphones are not approved medical devices, this means that they can not be the primary way for the device to display you're result (i.e. an update in software could cause the app used to display the result to have a bug and not function correctly, which would have serious consequences) - I will have to look into the Dexcom system to see how they get around this!
They won't have the illustrated baggy jeans and football shirt either. ;-)The reasoning behind having a "watch-like" display rather than only using a smartphone is due to two reasons:
- Not all users will have a smartphone - especially elderly users
I prefer the type 3, more discreet. Now, there is alerady a non ivasive device, http://diatribe.org/abbott-freestyl...itoring-through-utter-simplicity-fingersticks
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