Fekal Con-Trate System

FDA 510(k) K830769 · Trend Scientific, Inc.

Substantially Equivalent

510(k) numberK830769

Submission

Device name
Fekal Con-Trate System
Applicant
Trend Scientific, Inc.
Mchenry, IL, US
Received
March 11, 1983
Decision date
April 5, 1983
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
K082638Advia Centaur System with Streamlab Analytical WorkcellKLI · Traditional Siemens Healthcare Diagnostics, Inc.02/26/2009SE
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

More from Biotecx Laboratories, Inc.

510(k)DeviceDecision
K954996Trend Amebiasis (E.Histolytica) Serological Elisa Test SystemKHW · Traditional 08/08/1996SE
K955755Trend Cryptosporidium Detection Test SystemsMHJ · Traditional 07/11/1996SE
K952467Trend Giardia Lamblia Direct Detection System (Modified Kit)MHI · Traditional 11/20/1995SE
K953284Trend Giardia Direct Detection RS Test SystemMHI · Traditional 10/06/1995SE
K862914Fekal Check Parasitology Control SlideJTR · Traditional 09/16/1986SE

Questions and answers

When was Fekal Con-Trate System cleared by the FDA?

Fekal Con-Trate System (K830769) received a 510(k) decision of Substantially Equivalent on April 5, 1983, 25 days after the submission was received.

What is the product code of K830769?

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