Enzyme-Test TBC T4 Uptake

FDA 510(k) K820879 · Icl Scientific

Substantially Equivalent

510(k) numberK820879

Submission

Device name
Enzyme-Test TBC T4 Uptake
Applicant
Icl Scientific
Mchenry, IL, US
Received
March 30, 1982
Decision date
April 16, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KHQ – Radioassay, Triiodothyronine Uptake
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1715
Specialty
Clinical Chemistry

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K981375Ace T Uptake Reagent Tu CalibratorsKHQ · Traditional Schiapparelli Biosystems, Inc.06/10/1998SE
K980088T-Uptake Microplate EiaKHQ · Traditional Monobind02/04/1998SE
K970539Chiron Diagnostics ACS:180TU PKHQ · Traditional Chiron Diagnostics Corp.03/24/1997SE
K964308Vitros Immunodiagnostics Products T3 Uptake Reagent Pack (GEM.1025) and T3 Uptake…KHQ · Traditional Johnson & Johnson Clinical Diagnostics, Inc.11/27/1996SE
K961488Elecsys T-Uptake AssayKHQ · Traditional Boehringer Mannheim Corp.06/12/1996SE
K954807Cedia T Uptake AssayKHQ · Traditional Boehringer Mannheim Corp.12/21/1995SE
K951586T-Uptake Eia TestKHQ · Traditional Diagnostic Reagents, Inc.05/15/1995SE
K933414Stratus(R) Thyroid Uptake Fluor Enzyme ImmunoassayKHQ · Traditional Baxter Diagnostics, Inc.11/22/1994SE
K934312Axsym(Tm) T-UptakeKHQ · Traditional Abbott Laboratories06/21/1994SE
K935816Vidas T UptakeKHQ · Traditional Biomerieux Vitek, Inc.03/22/1994SE

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K832823Enzymune-Test TSHJLW · Traditional 10/14/1983SE
K831383Event-Test SlideJHJ · Traditional 06/22/1983SE
K823199Enzyme-Test DigoxinKXT · Traditional 11/29/1982SE
K822777Therapeutic Drug ControlDIF · Traditional 10/08/1982SE
K822346Histimune Enzyme-Ana TestLJM · Traditional 10/08/1982SE
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Questions and answers

When was Enzyme-Test TBC T4 Uptake cleared by the FDA?

Enzyme-Test TBC T4 Uptake (K820879) received a 510(k) decision of Substantially Equivalent on April 16, 1982, 17 days after the submission was received.

What is the product code of K820879?

The FDA product code is KHQ – Radioassay, Triiodothyronine Uptake, a Class II (moderate risk) device regulated under 21 CFR 862.1715.