So yeah, a couple of things. So first of all, FDA clearance depends on the indication of use, as you mentioned, right? That's all that is, right? So indication of use is governed by the application that the model is being used in. So they don't approve models, they approve applications being used for clinical care of any sort, right? Be it segmentation, as you said. So it's all about the indication of use and various different guidelines and regulatory process have been defined based on how those approval happen. The way it happens is there's a completely brand new indication, a brand new use case, usually goes through a de novo process. And de novo process then leads to a creation of regulation on how they will be assessed going forward. If you talk to any of the FDA senior leadership, they will agree with you 100 % that this model was initially designed on top of a drug approval model in the early days of CADE, which was very deterministic. know, weren't machine learning models, breast CAD is how all things started. And what has happened is because of the risk and cost and all this stuff, lot of people have built applications using those old frameworks to get it through the FDM, right? So now the problem is for this to change, requires Congress, you know, legislation changes. And I don't know, with all the pressures, a number or MTA, this is the right time anybody is going to go through and try to change the regulations.