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This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.
88364-If additional probe stain, in situ
|Test ID||Test Order Name||Order LOINC Code|
|80786||Epstein Barr Virus, In Situ Hybrid||In Process|
|Result ID||Test Result Name||Result LOINC Code|
|18857||Accession Number||No LOINC Needed|
|18859||Ref Path/Phys Address||74221-3|
|18860||Material:||No LOINC Needed|
|18862||SP Signing Pathologist:||19139-5|
|18863||*Previous Report Follows*||No LOINC Needed|