ALPHA-2 Macroglobulin Test Rid Kit

FDA 510(k) K914389 · The Binding Site, Ltd.

Substantially Equivalent

510(k) numberK914389

Submission

Device name
ALPHA-2 Macroglobulin Test Rid Kit
Applicant
The Binding Site, Ltd.
Los Angeles, CA, US
Received
October 1, 1991
Decision date
December 20, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DEB – Alpha-2-Macroglobulin, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5620
Specialty
Immunology

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K974564Immage Immunochemistry System ALPHA-2-MACROGLOBULIN ReagentDEB · Traditional Beckman Instruments, Inc.02/17/1998SE
K896483QM300 ALPHA2 Macroglobulin Antibody PackDEB · Traditional Kallestad Diag, A Div. of Erbamont, Inc.12/01/1989SE
K85068372 Determ. Size Radial Immunodiffusion Test ALPHA2DEB · Traditional Kent Laboratories, Inc.11/27/1985SE
K851282Radial Immunodiffusion Plates ALPHA-2 MacroglobuliDEB · Traditional Cooper Biomedical, Inc.05/24/1985SE
K850603SPQ Test System for ALPHA(2) MacroglobulinDEB · Traditional Applications Lab03/05/1985SE
K812493Immunogl. Frct. of Rabbit Antiser.-MacroDEB · Traditional Dako Corp.09/23/1981SE
K791340Human ALPHA2 MacroglobulinDEB · Traditional Beckman Instruments, Inc.08/16/1979SE

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Questions and answers

When was ALPHA-2 Macroglobulin Test Rid Kit cleared by the FDA?

ALPHA-2 Macroglobulin Test Rid Kit (K914389) received a 510(k) decision of Substantially Equivalent on December 20, 1991, 80 days after the submission was received.

What is the product code of K914389?

The FDA product code is DEB – Alpha-2-Macroglobulin, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5620.