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This test uses a standard method. 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 Value|
|60483||HPV High Risk, DNA ISH||In Process|
|Result ID||Test Result Name||Result LOINC Value|
|20353||Accession Number||No LOINC Needed|
|20355||Ref Path/Phys Address||74221-3|
|20356||Material:||No LOINC Needed|
|20360||SP Signing Pathologist:||19139-5|
|20361||*Previous Report Follows*||No LOINC Needed|