Ann: FDA Update for CONNEQT Companion App, page-9

  1. 2,733 Posts.
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    You’ve got me thinking.

    Im assuming the Conneqt Pulse device is heavily dependent on the Conneqt App. The pulse is designed to deliver 8 new biometric readings, never seen before ( if my memory serves me correctly … I’m in a coffee shop typing this! ) . I imagine if the Pulse needs to connect to the app to complete the readings and generate data then this would all be part of the submission. Could it be that the app needed clearance ( or at least designation assigned ) before Andon could complete the Pulse submission?

    Maybe this is the all clear they needed ?Interested in thoughts if any regulatory contributors out there.
 
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