Rover Mobile X-ray US FDA 510(K) Submission

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.”

 

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