Rover Mobile X-ray US FDA 510(K) Submission
Micro-X’s Managing Director, Peter Rowland, commented:
“We are very pleased to have submitted Micro-X’s first 510(k) application under its own name to the FDA. Obtaining FDA regulatory clearance is a key milestone of ours in 2020 as we are planning and building towards the launch of the Rover as our second commercial product later this year.”
