QM300 ALPHA2 Macroglobulin Antibody Pack

FDA 510(k) K896483 · Kallestad Diag, A Div. of Erbamont, Inc.

Substantially Equivalent

510(k) numberK896483

Submission

Device name
QM300 ALPHA2 Macroglobulin Antibody Pack
Applicant
Kallestad Diag, A Div. of Erbamont, Inc.
Chaska, MN, US
Received
November 13, 1989
Decision date
December 1, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K053073N Antisera to Human ALPHA2-MACROGLOBULINDEB · Traditional Dade Behring, Inc.03/28/2006SE
K974564Immage Immunochemistry System ALPHA-2-MACROGLOBULIN ReagentDEB · Traditional Beckman Instruments, Inc.02/17/1998SE
K914389ALPHA-2 Macroglobulin Test Rid KitDEB · Traditional The Binding Site, Ltd.12/20/1991SE
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 QM300 ALPHA2 Macroglobulin Antibody Pack cleared by the FDA?

QM300 ALPHA2 Macroglobulin Antibody Pack (K896483) received a 510(k) decision of Substantially Equivalent on December 1, 1989, 18 days after the submission was received.

What is the product code of K896483?

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