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Test ID: FCP12    
Cytokine Panel 12

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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 and its performance characteristics determined by ARUP Laboratories. The U.S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.

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.

83520 x12

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
Z2731Tumor Necrosis Factor - alphaIn Process
Z2732Interleukin 2In Process
Z2721Interleukin 2 Receptor CD25 SolubleIn Process
Z2722Interleukin 12In Process
Z2723Interferon gammaIn Process
Z2724Interleukin 4In Process
Z2725Interleukin 5In Process
Z2726Interleukin 10In Process
Z2727Interleukin 13In Process
Z2728Interleukin 1 betaIn Process
Z2729Interleukin 6In Process
Z2730Interleukin 8In Process