Leukemia/Lymphoma Immunophenotyping by Flow Cytometry, Tissue
Fees Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
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 Laboratory Medicine and Pathology, Mayo Clinic. This test has not been cleared or approved by the U.S. Food and Drug Administration.
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 ID||Reporting Name||LOINC Code|
|19564||Ref Path/Phys Address||74221-3|
|19565||Place of Death:||21987-3|
|19566||Date and Time of Death:||31211-6|
|19567||Date of Autopsy:||In Process|
|19571||Microscopic Description:||In Process|
|19572||Clinical History:||In Process|
|19579||SP Signing Pathologist:||N/A|
|19580||*Previous Report Follows*||N/A|