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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.
|Test ID||Test Order Name||Order LOINC Code|
|8041||Cutaneous Immunofluorescence, Bx||In Process|
|Result ID||Test Result Name||Result LOINC Code|
|18603||Accession Number||No LOINC Needed|
|18605||Ref Path/Phys Address||74221-3|
|18606||Anatomic Site of Tissue:||39111-0|
|18610||SP Signing Pathologist:||19139-5|
|18611||*Previous Report Follows*||No LOINC Needed|