There’s an article in the other thread suggesting that the FDA’s big problem with the Enlite is that the > 3 day settings require the users to “override” the 3 day limit for sensors programmed into the current MM sensor software? So they won’t approve it. That, plus Blue Cross citing the FDA as saying 200 strips/ day is what I need has vaulted them to the top of my least favorite federal organization list.
The other thread is here: https://forum.tudiabetes.org/topics/medtronic-launches-enlite