A 60-day appeal window has passed for the Food and Drug Administration to appeal a federal court ruling that invalidated its final rule to regulate laboratory-developed tests as medical devices, effectively eliminating it. The rule, issued last year, would have phased out its general enforcement discretion approach for most lab-developed tests over four years. The U.S. District Court for the Eastern District of Texas struck down the rule in a decision March 31. 
 
The AHA previously expressed concerns about the rule when it was proposed and urged the FDA not to apply it to hospital and health system lab-developed tests.

Related News Articles

Headline
The U.S. District Court for the Eastern District of Texas March 31 ruled that the Food and Drug Administration does not have the authority to regulate…
Headline
The Food and Drug Administration April 29 issued a final rule that would phase out its general enforcement discretion approach for most laboratory developed…
Headline
The Food and Drug Administration’s proposal to regulate laboratory developed tests would undermine innovation and reduce access to effective and appropriate…
Headline
The Food and Drug Administration’s proposal to regulate laboratory developed tests would undermine innovation and reduce access to effective and appropriate…
Headline
AHA Dec. 1 urged the Food and Drug Administration not to apply its device regulations to hospital and health system laboratory developed tests. Commenting…