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Test ID: FPNAP    
Pneumococcal Antibody Panel (12 Serotype)

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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 Viracor-IBT Laboratories. It has not been cleared or approved by the FDA.

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.

86317 x 12

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
FPNAPPneumococcal Antibody Panel (12 Serotype)In Process


Result IDTest Result NameResult LOINC Code
Z3132Pneumo Ab Type 127227-8
Z3133Pneumo Ab Type 3In Process
Z3134Pneumo Ab Type 4In Process
Z3135Pneumo Ab Type 8In Process
Z3136Pneumo Ab Type 9 (9N)In Process
Z3137Pneumo Ab Type 12 (12F)In Process
Z3138Pneumo Ab Type 14In Process
Z3139Pneumo Ab Type 19 (19F)In Process
Z3140Pneumo Ab Type 23 (23F)In Process
Z3141Pneumo Ab Type 26 (6B)In Process
Z3142Pneumo Ab Type 51 (7F)In Process
Z3143Pneumo Ab Type 56 (18C)In Process

LOINC and CPT codes are provided by the performing laboratory.