Epsilon Ige Test Kit

FDA 510(k) K831987 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK831987

Submission

Device name
Epsilon Ige Test Kit
Applicant
Beckman Instruments, Inc.
Walker, MI, US
Received
June 21, 1983
Decision date
October 14, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DGO – Ige, Peroxidase, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5510
Specialty
Immunology

Other 510(k)s with product code DGO

510(k)DeviceApplicantDecision
K943194Immulite(R) Allergy Food Panel FP5EDGO · Traditional Diagnostic Products Corp.02/23/1995SE
K920087Ige Eia Test KitDGO · Traditional The Binding Site, Ltd.09/14/1992SE
K911511Alastat Allergen Specified Ige System, ModifiedDGO · Traditional Diagnostic Products Corp.04/17/1991SE
K894039Quidel Total Ige Test Quantitative VersionDGO · Traditional Quidel Corp.07/14/1989SE
K893125Beckman Epsilon(Tm) Ige Reagent KitDGO · Traditional Beckman Instruments, Inc.06/16/1989SE
K872801Alleia Total Ige Eia W/Mono Anti. EKIE1, 2, 5DGO · Traditional Diagnostic Products Corp.09/10/1987SE
K860851Allegro Ige Enzyme Immunoassay SystemDGO · Traditional Nichols Institute Diagnostics03/28/1986SE
K853607Allerg-E Ige Enzyme Immunoassay KitDGO · Traditional Dexall Biomedical Labs, Inc.11/07/1985SE
K831984Polystyrene Micro-Liter Plate-BirchtreeDGO · Traditional Diagnostic Reagent Tech.11/21/1983SE
K831774Logipe a Data Reducsystem Ip Specific-DGO · Traditional Diagnostic Reagent Tech.07/18/1983SE

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Questions and answers

When was Epsilon Ige Test Kit cleared by the FDA?

Epsilon Ige Test Kit (K831987) received a 510(k) decision of Substantially Equivalent on October 14, 1983, 115 days after the submission was received.

What is the product code of K831987?

The FDA product code is DGO – Ige, Peroxidase, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5510.