Carbamezepine Reagent Test Kit

FDA 510(k) K831222 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK831222

Submission

Device name
Carbamezepine Reagent Test Kit
Applicant
Beckman Instruments, Inc.
Mchenry, IL, US
Received
April 15, 1983
Decision date
May 9, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KLT – Enzyme Immunoassay, Carbamazepine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3645
Specialty
Clinical Toxicology

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K063131Carbamazepine, Valproic Acid, TDM Calibration Set B and Abtrol, Nortrol ControlsKLT · Traditional Thermo Electron OY10/05/2007SE
K042808Advia Ims Carbamazepine MethodKLT · Traditional Bayer Healthcare, LLC02/08/2005SE
K031902Online TDM CarbamazepineKLT · Traditional Roche Diagnostics Corp.09/17/2003SE
K011648Randox CarbamazepineKLT · Traditional Randox Laboratories, Ltd.01/15/2002SE
K010814Emit 2000 Carbamazepine Assay, Model OSR4F229KLT · Special Syva Co., Dade Behring, Inc.04/13/2001SE
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K000007Immulite Carbamazepine, Immulite 2000 Carbamazepine, Catalog # LKCB1, LKCB5 & L2KCB2…KLT · Traditional Diagnostic Products Corp.02/28/2000SE

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Questions and answers

When was Carbamezepine Reagent Test Kit cleared by the FDA?

Carbamezepine Reagent Test Kit (K831222) received a 510(k) decision of Substantially Equivalent on May 9, 1983, 24 days after the submission was received.

What is the product code of K831222?

The FDA product code is KLT – Enzyme Immunoassay, Carbamazepine, a Class II (moderate risk) device regulated under 21 CFR 862.3645.