Test for Human Alpha One Acid Glyco-

FDA 510(k) K831960 · Kent Laboratories, Inc.

Substantially Equivalent

510(k) numberK831960

Submission

Device name
Test for Human Alpha One Acid Glyco-
Applicant
Kent Laboratories, Inc.
Mchenry, IL, US
Received
June 17, 1983
Decision date
July 19, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LKL – Alpha-1-Acid-Glycoprotein, Antigen, Antiserum, Control
Device class
Class I (low risk)
Regulation
21 CFR 866.5420
Specialty
Immunology

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K993441K-Assay ALPHA-1 AGLKL · Traditional Kamiya Biomedical Co.11/24/1999SE
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K964257Immage Immunochemistry System ALPHA-1-ACID Glycoprotein (Aag) ReagentLKL · Traditional Beckman Instruments, Inc.03/24/1997SE
K922417Al-Acid Glycoprotein Rid KitLKL · Traditional The Binding Site, Ltd.08/20/1992SE
K904175Raichem (TM) Spia (TM) - Acid Glycoprotein ReagentLKL · Traditional Reagents Applications, Inc.11/13/1990SE
K884217Technicon DPA-1 Analyte Alpha 1 Acid GlycoproteinLKL · Traditional Technicon Instruments Corp.11/04/1988SE
K873868ALPHA-1-ACID Glycoprotein (Orosomucoid)LKL · Traditional Unipath , Ltd.10/20/1987SE
K862087Santest 1APLKL · Traditional Scientific Sales Intl., Inc.12/03/1986SE
K861336Iap Plate TestLKL · Traditional Scientific Sales Intl., Inc.04/25/1986SE
K841734Tago Fiffu-Gen, OrosomucoidLKL · Traditional Tago, Inc.06/01/1984SE

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K85068372 Determ. Size Radial Immunodiffusion Test ALPHA2DEB · Traditional 11/27/1985SE
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K850691Antiserum to Human Apolipoprotein A-IMSJ · Traditional 11/01/1985SE
K850690Antiserum to Human Apolipoprotein BMSJ · Traditional 11/01/1985SE
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Questions and answers

When was Test for Human Alpha One Acid Glyco- cleared by the FDA?

Test for Human Alpha One Acid Glyco- (K831960) received a 510(k) decision of Substantially Equivalent on July 19, 1983, 32 days after the submission was received.

What is the product code of K831960?

The FDA product code is LKL – Alpha-1-Acid-Glycoprotein, Antigen, Antiserum, Control, a Class I (low risk) device regulated under 21 CFR 866.5420.