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Test ID: 80172    
Human Papillomavirus (HPV) Typing, DNA In Situ Hybridization

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Test Classification Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.

This test uses a standard method. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.


88364-If additional probe stain, in situ

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and result codes of this test.

Test IDTest Order NameOrder LOINC Code
80172Human Papillomavirus (HPV) Typing, DNA In Situ HybridizationIn Process


Result IDTest Result NameResult LOINC Code
18754Accession NumberNo LOINC Needed
18755Referring Pathologist/Physician46608-6
18756Ref Path/Phys Address74221-3
18757Material:No LOINC Needed
18759SP Signing Pathologist:19139-5
18760*Previous Report Follows*No LOINC Needed
19218Addendum Comment:22638-1
18762Addendum Pathologist:19139-5

LOINC and CPT codes are provided by the performing laboratory.