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Test ID: 89118    
ThinPrep Screen with HPV for Women 30 Years and Older

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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 has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified 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.

ThinPrep Screen with HPV for Women 30 Years and Older

G0123-(Government payers)/ThinPrep Manual Screen

88142-(All other payers)/ThinPrep Manual Screen

 

Human Papillomavirus (HPV) Detection-High Risk Types

87621

 

Physician Interpretation of ThinPrep, PAP

G0124-(Government payers)/ (if appropriate)

88141-(All other payers)/ (if appropriate)

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

Result IDReporting NameLOINC Code
19795Accession NumberN/A
19796Final Diagnosis22637-3
19797CytotechnologistN/A
19798Revision DescriptionN/A
19799Signing Pathologist19139-5
19800Specimen Description:33511-7
19801*Previous Report Follows*N/A
19802Addendum35265-8
19803Addendum Comment:22638-1