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Test ID: FEYE    
Uveal Melanoma, Chromosome 3 Monosomy, FISH, Tissue

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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 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.

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.

Uveal Melanoma, Chromosome 3 Monosomy, FISH, Tissue

88271 x 2-DNA probe, each

88275-Interphase in situ hybridization, 100-300 cells

88291-Interpretation and report

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
29674SpecimenN/A
29675Specimen IDN/A
29676Source31208-2
29677Order DateN/A
CG081Reason For Referral42349-1
29679Method49549-9
29680ResultIn Process
29681Interpretation69965-2
29682AmendmentIn Process
29683Reviewed ByN/A
29684Release DateN/A