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It was developed in response to data analysis indicating that there was a significant difference in CCRs for those hospitals with and without blood-specific cost centers and past public comments indicating that the former OPPS policy of defaulting to the overall hospital CCR for hospitals not reporting a blood-specific cost center often resulted in an underestimation of the true hospital costs for blood and blood products

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The commenter also noted that 1 month after C1747 was established based on the approval of the STERIS Uretero1 TM device pass-through application, FDA granted the LithoVue TM Elite System 510(k) clearance, on February 2, 2023

This compound is frequently investigated for its involvement in fatty-acid oxidation, ATP-energy production, metabolic-efficiency signalling, and exercise-performance research