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Test ID FHIST MVista Histoplasma Ag Quantitative, Serum

Method Name

Enzyme Immunoassay (EIA)

Reporting Name

MVista Histoplasma Ag, S

Specimen Type


Specimen Required

Specimen Type: Serum

Container/Tube: Red or SST

Specimen Volume: 2 mL

Collection Instructions: Draw blood in a plain red-top tube(s). (Serum gel tube is acceptable.) Spin down and send 2 mL serum refrigerate in a plastic vial

Specimen Minimum Volume

1.2 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 14 days
  Ambient  14 days

Reference Values

Reference interval:         None Detected


Results reported as ng/mL in 0.4 – 19.0 ng/mL range


Results above the limit of detection, but below 0.4 ng/mL are reported as 'Positive, Below the Limit of Quantitation'.


Results above 19.0 ng/mL are reported as 'Positive, Above the Limit of Quantitation'.


Day(s) and Time(s) Performed

Monday through Friday

Performing Laboratory

MiraVista Diagnostics

CPT Code Information


LOINC Code Information

Test ID Test Order Name Order LOINC Value
FHIST MVista Histoplasma Ag, S 51753-2


Result ID Test Result Name Result LOINC Value
Z1711 Result: 51753-2
Z1035 Interpretation Not Provided

Test Classification

This test was developed and its performance characteristics determined by MiraVista Diagnostics. It has not been cleared or approved by the FDA; 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.

NY State Approved