IMMULITE 2000 3gAllergy Specific IgE Vantage; IMMULITE 2000 Systems Peanut Allergen (F13)

FDA 510(k) K260331 · Siemens Healthcare Diagnostics Products, Ltd.

Substantially Equivalent

510(k) numberK260331

Submission

Device name
IMMULITE 2000 3gAllergy Specific IgE Vantage; IMMULITE 2000 Systems Peanut Allergen (F13)
Applicant
Siemens Healthcare Diagnostics Products, Ltd.
Llanberis, GB
Received
February 2, 2026
Decision date
September 4, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DHB – System, Test, Radioallergosorbent (Rast) Immunological
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5750
Specialty
Immunology

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K260280NOVEOS Specific IgE (sIgE); Capture Reagent F004, Wheat (Triticum aestivum); Capture…DHB · Traditional Hycor Biomedical06/18/2026SE
K260059NOVEOS Specific IgE (sIgE); Capture Reagent F018, Brazil Nut (Bertholletia excelsa)…DHB · Traditional Hycor Biomedical05/15/2026SE
K252775NOVEOS Specific IgE (sIgE): Capture Reagent F013, Peanut (Arachis hypogaea); Capture…DHB · Traditional Hycor Biomedical01/16/2026SE
K252493NOVEOS Specific IgE (sIgE); Capture Reagent F024, Shrimp (Shrimp spp.); Capture Reagent…DHB · Traditional Hycor Biomedical12/23/2025SE
K242531NOVEOS Specific IgE (sIgE) Assay; Capture Reagent G010, Johnson Grass (Sorghum…DHB · Traditional Hycor Biomedical04/23/2025SE
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Questions and answers

When was IMMULITE 2000 3gAllergy Specific IgE Vantage; IMMULITE 2000 Systems Peanut Allergen (F13) cleared by the FDA?

IMMULITE 2000 3gAllergy Specific IgE Vantage; IMMULITE 2000 Systems Peanut Allergen (F13) (K260331) received a 510(k) decision of Substantially Equivalent on September 4, 2026, 214 days after the submission was received.

What is the product code of K260331?

The FDA product code is DHB – System, Test, Radioallergosorbent (Rast) Immunological, a Class II (moderate risk) device regulated under 21 CFR 866.5750.