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Similar to our discussion in the FY 2023 IPPS/LTCH PPS proposed rule (87 FR 28308), we note that although the applicant states that XENOVIEW TM has not been assigned to an MS-DRG and cannot be compared to an existing technology, we believe that based on its FDA indication, cases involving the use of XENOVIEW TM would be assigned to the same MS-DRGs as cases involving the use of other MRIs and imaging modalities for pulmonary function and imaging of the lungs

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