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This test was developed and its performance characteristics 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-GC, each additional probe stain, in situ
|Result ID||Reporting Name||LOINC Code|
|18756||Ref Path/Phys Address||74221-3|
|18759||SP Signing Pathologist:||In Process|
|18760||*Previous Report Follows*||N/A|
LOINC and CPT codes are provided by the performing laboratory.