Device typeAllergen-specific immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA): A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin E (IgE) antibodies to one or multiple allergen(s) in a clinical specimen, using an enzyme immunoassay (EIA) method. It is typically used to screen for allergies associated with certain conditions (e.g., food intolerance).
FDA categorySYSTEM, TEST, RADIOALLERGOSORBENT (RAST) IMMUNOLOGICAL
Device ID07333066005553
Catalog number14-4965-01
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information