Determ. Size 72 Radial Human Haptoglob

FDA 510(k) K831957 · Kent Laboratories, Inc.

Substantially Equivalent

510(k) numberK831957

Submission

Device name
Determ. Size 72 Radial Human Haptoglob
Applicant
Kent Laboratories, Inc.
Mchenry, IL, US
Received
June 17, 1983
Decision date
July 18, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DAD – Haptoglobin, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5460
Specialty
Immunology

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K963286Immage Immunochemistry System Haptoglobin (HPT) ReagentDAD · Traditional Beckman Instruments, Inc.10/07/1996SE
K952593N/T Protein Control Sy/L, M and HDAD · Traditional Behring Diagnostics, Inc.07/17/1995SE
K915829Il Test(Tm) Haptoglobin (HPT)DAD · Traditional Instrumentation Laboratory CO07/29/1992SE
K911898Raichem(Tm) Spia(Tm) Haptoglobin ReagentDAD · Traditional Reagents Applications, Inc.05/08/1991SE
K890562Spq(Tm) Antibody Reagent Set II for HPTDAD · Traditional Atlantic Antibodies02/22/1989SE
K873866HaptoglobinDAD · Traditional Unipath , Ltd.10/20/1987SE
K872717QM300 Haptoglobin Antibody PackDAD · Traditional Kallestad Diag, A Div. of Erbamont, Inc.07/21/1987SE

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K951967Human C1 Inactivator or C-1 Esterase Inhibitor Radial Immunodiffusion KitDBA · Traditional 05/30/1995SE
K950102Human C-5 Radial Immunodiffusion KitDAY · Traditional 04/10/1995SE
K85068372 Determ. Size Radial Immunodiffusion Test ALPHA2DEB · Traditional 11/27/1985SE
K85068272 Determ. Size Radial Immuno. Test Human CeruloplDDB · Traditional 11/25/1985SE
K850691Antiserum to Human Apolipoprotein A-IMSJ · Traditional 11/01/1985SE
K850690Antiserum to Human Apolipoprotein BMSJ · Traditional 11/01/1985SE
K850686Antiserum to Human PrealbuminJZJ · Traditional 11/01/1985SE
K831961Immunodiffusion Test Human AntithrombinJBQ · Traditional 08/11/1983SE

Questions and answers

When was Determ. Size 72 Radial Human Haptoglob cleared by the FDA?

Determ. Size 72 Radial Human Haptoglob (K831957) received a 510(k) decision of Substantially Equivalent on July 18, 1983, 31 days after the submission was received.

What is the product code of K831957?

The FDA product code is DAD – Haptoglobin, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5460.