Technicon RA-1000 Sys T4-THYROXINE

FDA 510(k) K841576 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK841576

Submission

Device name
Technicon RA-1000 Sys T4-THYROXINE
Applicant
Technicon Instruments Corp.
Mchenry, IL, US
Received
April 17, 1984
Decision date
May 22, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KLI – Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1700
Specialty
Clinical Chemistry

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K103484GSP Neonatal Thyroxine (T4)KLI · Traditional Wallac Oy, A Subsidiary of Perkinelmer, Inc.04/22/2011SE
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K030860Accubind Neonatal T4 Microplate Eia, Model 2625-300KLI · Traditional Monobind08/22/2003SE
K023369Access Total T4 AssayKLI · Traditional Beckman Coulter, Inc.12/09/2002SE
K001603Reprobead T4 Enzyme Immunoassay Reagent Kit (Catalog# 105)KLI · Traditional Repromedix Corp.10/05/2000SE
K000600Syva Emit 2000 Thyroxine Assay, CalibratorsKLI · Traditional Syva Co., Dade Behring, Inc.03/27/2000SE
K991432Biocheck Total T4 Enzyme Immunoassay Test Kit, Model BC-1007KLI · Traditional Biocheck, Inc.06/02/1999SE
K982298Opticoat T4 Eia KitKLI · Traditional Biotecx Laboratories, Inc.02/03/1999SE

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Questions and answers

When was Technicon RA-1000 Sys T4-THYROXINE cleared by the FDA?

Technicon RA-1000 Sys T4-THYROXINE (K841576) received a 510(k) decision of Substantially Equivalent on May 22, 1984, 35 days after the submission was received.

What is the product code of K841576?

The FDA product code is KLI – Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine, a Class II (moderate risk) device regulated under 21 CFR 862.1700.