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Test ID: FMY3P    
Myositis Ab 3 Panel, Extensive

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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 validated by RDL Inc. The FDA has determined that approval for this test is not necessary. This is an analyte specific reagent (ASR) test.

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

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.

86235-Anti-Jo 1 Ab

83516-MI-2

83516-PL-7

83516-PL-12

83516-EJ

83516-OJ

83516-SRP

83516-KU

83516-U2 SN RNP

83516-P140

83516-P155/140

83516-Fibrillarin U3

86235-PM/SCL

86235-SSA 52 KD AB IgG

86235-U1 RNP

86235-RNP AB

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
Z2577MI-2In Process
Z2578JO-1In Process
Z2579PL-7In Process
Z2580PL-12In Process
Z2581EJIn Process
Z2582OJIn Process
Z2583SRPIn Process
Z2584P155/140In Process
Z2585P140In Process
Z2586KUIn Process
Z2587U1 RNP ABIn Process
Z2588RNP ABIn Process
Z2589PM/SCLIn Process
Z2590Fibrillarin U3In Process
Z2591SSA52 KD Ab, IGGIn Process
Z2592U2 SN RNPIn Process