Guided Therapeutics Inc (GTHP)

[GetSeriousOK]

If SMI runs any kind of meaningful clinical trial, Guided could use it in their FDA submission.

I'm not saying SMI will accomplish this task. BUT if they do.... the timing could be advantageous.

Realistically... the CFDA would probably accept Guided's new USA clinical trial when it's completed. A clinical trial doesn't have to be conducted in the country of regulatory clearance. For that matter, SMI or Shenghuo could have submitted Guided's trials four years ago, just to open the door with the CFDA or maybe even get approval.

We still don't know whether the CFDA considers the LuViva Scan to be Class II or Class III.