Device typeAllergen-specific/total immunoglobulin E (IgE) antibody IVD, control: A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of immunoglobulin E (IgE) antibodies to one or multiple allergens and total immunoglobulin E (IgE total) antibodies in a clinical specimen.
FDA categorySYSTEM, TEST, RADIOALLERGOSORBENT (RAST) IMMUNOLOGICAL
Device ID00813382010181
Catalog number94173
AvailabilityPrescription
Single useYes
MRI safetyLabeling does not contain MRI Safety Information