Quidel Allergy Screen

FDA 510(k) K883666 · Quidel Corp.

Substantially Equivalent

510(k) numberK883666

Submission

Device name
Quidel Allergy Screen
Applicant
Quidel Corp.
San Diego, CA, US
Received
August 26, 1988
Decision date
October 18, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

Other 510(k)s with product code DHB

510(k)DeviceApplicantDecision
K260331IMMULITE 2000 3gAllergy Specific IgE Vantage; IMMULITE 2000 Systems Peanut Allergen (F13)DHB · Traditional Siemens Healthcare Diagnostics Products, Ltd.09/04/2026SE
K261027NOVEOS Specific IgE (sIgE); Capture Reagent F014, Soybean (Glycine max); Capture Reagent…DHB · Traditional Hycor Biomedical07/24/2026SE
K260591NOVEOS Specific IgE (sIgE);Capture Reagent F010, Sesame Seed (Sesamum indicum);Capture…DHB · Traditional Hycor Biomedical07/21/2026SE
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
K212181ImmunoCAP Allergen f433, Allergen component rTri a 14 LTP, Wheat, ImmunoCAP Allergen…DHB · Traditional Phadia AB08/03/2022SE
K220162Noveos Immunoanalyzer System, Noveos Specific IgE (sIgE), Capture Reagent M006, AlternariaDHB · Traditional Hycor Biomedical02/18/2022SE

More from Hycor Biomedical

510(k)DeviceDecision
K231795QuickVue COVID-19 TestQYT · Traditional 03/22/2024SE
K232286Savanna HSV 1+2/VZV Assay, Savanna HSV 1+2/VZV Control Set, Savanna InstrumentPGI · Traditional 12/20/2023SE
K233688Sofia 2 SARS Antigen+ FIA; Sofia 2 SARS Antigen+ FIA Control Swab SetQVF · Special 12/13/2023SE
K230349Lyra RSV+hMPV AssayOEM · Special 03/10/2023SE
K230236Lyra Influenza A+B AssayOZE · Special 03/03/2023SE
K211342Sofia 2 Campylobacter FIALQP · Traditional 11/23/2021SE
K173496Sofia 2 Lyme FIA, Sofia Lyme Control SetLSR · Dual Track 08/30/2018SE
K181029Solana Bordetella Complete AssayOZZ · Traditional 07/15/2018SE
K173691Sofia Lyme FIA, Sofia 2 analyzer, Sofia 2 Installation PackLSR · Traditional 02/28/2018SE
K180288QuickVue Influenza A+BPSZ · Special 02/13/2018SE

Questions and answers

When was Quidel Allergy Screen cleared by the FDA?

Quidel Allergy Screen (K883666) received a 510(k) decision of Substantially Equivalent on October 18, 1988, 53 days after the submission was received.

What is the product code of K883666?

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